Author Topic: The research chemical thread  (Read 771 times)

Naf1

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The research chemical thread
« on: January 05, 2010, 12:50:22 AM »
As everyone should be aware there are a plethora of OTC research chemicals available online, this thread was to try and decipher the good from the down right dangerous from the potential precursors and also how to avoid some dodgy vendors and law enforcement honey pots while enjoying the quality produce on offer.

*      =  Recreational drug
**    =  Dangerous recreational drug
***  =  Potential presursor
****=  Pretty lethal

I will list some of the more common RC chems you will find nowdays(with wiki quotes), then will get vendor specific.

Methylenedioxy compounds;


Methylenedioxypyrovalerone (MDPV)*, is a psychoactive drug with stimulant and aphrodisiac properties which acts as a norepinephrine-dopamine reuptake inhibitor (NDRI), reportedly with four times the potency of methylphenidate (Ritalin, Concerta).

MDPV is not specifically listed as a controlled substance in any country besides Denmark. Some people have claimed that because MDPV is most closely related in molecular structure to a Schedule V drug (Pyrovalerone) in the US, it is not controlled by the Federal Analog Act.[citation needed] The law requires it to be an "analog" that is "substantially similar" to that of a Schedule I or II drug and intended for human consumption. There are no legal cases currently known of in the USA concerning MDPV. Prosecutors in a federal US court may claim MDPV is an analog of MDMA under the Federal Analog Act, although they could not claim it is an analog of Pyrovalerone since it is not a Schedule I or II controlled substance. The prosecution could be difficult however, because MDPV has a pentyl side chain where MDMA has a propyl side chain, MDPV a beta-ketone group where MDMA has two hydrogen atoms, and a pyrrolidine, cyclic, tertiary amine where MDMA has a simpler methylamino group, a primary amine. This distinction between primary amines and tertiary amines was a major determining factor in the decision that AET was not an analog of DMT or DET in the first case prosecuted under the Federal Analog Act. In its effects, MDPV is quite dissimilar to MDMA, with MDPV being a DA/NA reuptake inhibitor rather than a releaser, and MDPV apparently lacking the strong serotonergic activity of MDMA. It would probably be extremely difficult to find an expert witness willing to testify on a defendant's behalf.
Other drugs with a similar chemical structure include ?-pyrrolidinopropiophenone (?-PPP), which has a shorter alkyl chain and no ring substitution, pyrovalerone, which has a 4'-methyl group instead of a methylenedioxy ring, as well as analogues with between 3 and 6 carbons on the alkyl chain.[4]
These compounds have been reported as stimulants of abuse mainly in Germany and other European countries since the early 2000s, but they have remained generally vaguely known and rarely used illicitly or encountered by law enforcement.[5]
No deaths or injuries caused by this substance have been reported.


3,4-methylenedioxy-N-methylcathinone (MDMC, BK-MDMA)*, is a psychoactive drug of the phenethylamine-related Cathinone chemical class that acts as an entactogen, mild psychedelic and stimulant. It is the ?-keto analogue of 3,4-methylenedioxy-N-methylamphetamine (MDMA; "Ecstasy", "Adam", "Molly", "XTC").

MDMC is not explicitly scheduled in the United States (U.S.), but possession may still result in prosecution under the Federal Analog Act as an MDMA analogue. In New Zealand, although MDMC is not explicitly scheduled and falls outside the strict definitions of an "amphetamine analogue" in the Misuse of Drugs Act, it is considered to be "substantially similar" to methcathinone and is thus considered by law enforcement authorities to be a Class C illegal drug.
MDMC is currently not specifically mentioned in United Kingdom (U.K.) law as the ?-ketone is not covered under the Misuse of Drugs Act.
MDMC was sold in New Zealand for around 6 months from November 2005 to April 2006 as an MDMA substitute, under the name "Ease". The product was withdrawn after legal disputes with the government.


Butylone, ?-keto-N-methyl-3,4-benzodioxolylbutanamine (bk-MBDB)*,is a psychoactive drug and research chemical of the phenethylamine chemical class that acts as an entactogen, psychedelic, and stimulant. It is the ?-keto analogue of methylbenzodioxylbutanamine (MBDB).

Butylone was first synthesized by Koeppe, Ludwig and Zeile which is mentioned in their 1967 paper.[1] It remained an obscure product of academia until 2005 when it was synthesized by a chemical supply company, and has since continued to be sold as a designer drug.[2] It has since been explored as a possible entheogen. Butylone shares the same relationship to MBDB as methylone does to methylenedioxymethamphetamine (MDMA; "Ecstasy"). The dosage range is not fully understood but seems to be lower than for MBDB. Formal research on this chemical was first conducted in 2009, when it was shown to be metabolised in a similar manner to related drugs like methylone.


Phenethylamines;

Mephedrone or 4-methylmethcathinone or 4-methylephedrone (4-MMC)**, is a stimulant and entactogen drug of the phenethylamine, amphetamine, and cathinone chemical classes. It is sometimes sold as "plant food" online, is reported to be contained in some legal highs and is sometimes sold mixed with methylone, also known as “Bubbles”,[3] "miaow miaow", "Top Cat"[citation needed], or MMCAT.[4]
It has been reported that manufacturers are making "huge amounts of money" from selling the drug.

On December 14, 2008, an 18-year-old Swedish woman died in Stockholm after taking mephedrone in combination with other drugs. The 18-year-old and some friends took the substance in combination with cannabis on the night of Friday, 12 December. An ambulance was soon called to Bandhagen after the girl went into convulsions and turned blue in the face, Svenska Dagbladet reported.[18] Mephedrone was scheduled to be classified as a "dangerous substance" in Sweden even before the girl's death at Karolinska University Hospital on Sunday, 14 December, but the death brought much more media attention to the drug. The handling of mephedrone became classified as a criminal offence in Sweden on Monday 15 December (2008).4-Methylmethcathinone is unscheduled in the United States.Australia: Mephedrone is not specifically listed as prohibited in Australia, Federal Police have stated that it is an Analog to methcathinone and therefore illegal. No one in Australia has yet been charged with possession of mephedrone as authorities are divided over its legality.


2,5-dimethoxy-4-ethylthiophenethylamine (2C-T-2)*
I will let Shulgin tell the story, with a quote from Pihkal;
(with 25 mg) I was at a +++ in an hour! It is most difficult to do even ordinary things. I took notes but now I can't find them. This is much too high for anything creative, such as looking at pictures or trying to read. Talking is OK. And to my surprise I was able to get to sleep, and a good sleep, at the seven hour point.


2,5-dimethoxy-4-ethyl-phenethylamine (2C-E)*, is a psychedelic drug and phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin, sometimes used as an entheogen. 2C-E is typically sold as a white crystalline powder or in pill capsules.

It is commonly active in the 10–20 mg range, taken orally, and highly dose-sensitive. Insufflating (administering the chemical nasally) requires a much lower dose, typically not exceeding 5mgs, but this method of consumption elicits a noticeably painful or uncomfortable sensation in the nasal cavity for 10 minutes or so. Shulgin classified 2C-E as a member of the "magical half-dozen" in his book PiHKAL (Phenethylamines i Have Known And Loved). Many have reported that the general effects of 2C-E are similar to those of the other psychedelic phenethylamines, but far more intense. Vivid hallucinations similar to those experienced while under the influence of LSD are common, and many reports would indicate that the effects of this particular chemical may be overly intense for those not well experienced with psychedelics.
2C-E is unscheduled in the United States; however, there are currently several cases pending in U.S. federal court against vendors for selling research chemicals. These cases may address the question of whether this chemical could be legally defined as an analog of a scheduled substance.
It is a homologue of 2C-B, 2C-T-7 or mescaline (all three of which are scheduled substances), in which case sale for human consumption or possession to ingest or use for illicit non-medical or industrial intents and purposes could be prosecuted as crimes under the Federal Analog Act.

2,5-dimethoxy-4-iodophenethylamine (2C-I)*, is a psychedelic drug and phenethylamine of the 2C family.[1] It was first synthesized by Alexander Shulgin. It was described in Shulgin’s book PiHKAL (Phenethylamines i Have Known And Loved). The drug is used recreationally and as an entheogen but no medical or industrial uses have been reported yet. It is most commonly encountered in the form of its hydrochloride salt, a fluffy, sparkling white powder, and has also been pressed into tablet form.

2C-I is an illegal, controlled substance in several European nations, including Denmark, Germany, Greece, Ireland, the Netherlands, Poland, Spain and the United Kingdom.[4] In December 2003, the European Council issued a binding order compelling all EU member states to ban 2C-I within three months. 2C-I is unscheduled and unregulated in the United States, however its close similarity in structure and effects to 2C-B could potentially subject possession and sale of 2C-I to prosecution under the Federal Analog Act, if it is intended for human consumption. This seems to be the tactic the federal government is taking in the wake of the DEA's Operation Web Tryp.

Tryptamines:

O-Acetylpsilocin, 4-acetoxy-N,N-dimethyltryptamine, or 4-AcO-DMT*** and *, is a psychedelic (hallucinogenic). It is the acetylated form of the psychedelic mushroom alkaloid psilocin, and is a lower homologue of 4-AcO-DET and 4-AcO-DiPT. It may also be considered an analogue of psilocin, which is a Schedule I drug under the Controlled Substances Act of the USA, if there is evidence that it was being used for human consumption.

In the body 4-acetylpsilocin is evidently rapidly desacetylated to psilocin by acetylases and therefore has identical pharmacological properties to psilocin.

5-MeO-DMT (5-Methoxy-dimethyltryptamine), also known as O-Methylbufotenine (also see bufotenine)[*,is a powerful psychedelic tryptamine. It is found in a wide variety of plant and psychoactive toad species, and like its close relatives DMT and bufotenin (5-HO-DMT), it has been used as an entheogen by South American shamans for thousands of years.

On August 21, 2009, the DEA issued a Notice of Proposed Rulemaking to initiate placing 5-MeO-DMT into Schedule I of the Controlled Substances Act (the most restrictive category).[6] Comment DEA-2009-0008-0007.1 requested a 180 day extension of the period for public comment and requests for hearings, objected to the proposed rule on multiple grounds including Constitutional issues, identified the submitter as a person who would be "adversely affected and aggrieved by the proposed ruling" and requested an exemption for religious use if DEA did place 5-MeO-DMT in Schedule I "as an attempt to define and clarify some legal issues."[3]
On September 29 and 30, 2009, the DEA posted the Supporting & Related Materials for the NPRM while retaining the September 21, 2009 Due date for comments.[7]
On October 28, 2009 DEA reopened the period for public comment because it had not posted two Supporting & Related Materials documents online during the original period for public comment. Documents and comments were split between Docket ID: DEA-2009-0008 and Docket ID: DEA-2009-0013 in a manner which creates difficulty and in viewing all documents and determining where and how to submit comments online. The two Supporting & Related Materials documents were not posted to Docket ID: DEA-2009-0013 until November 3, 2009 but the 30 day period for public comment was not changed from November 27, 2009.

One company that stood out to be a law enforcement trap, would have to be '4 EVER RESEARCH' as they offer;

LSD 25,
Hydromorphone HCL,
Morphine sulfate,
Ketamine HCL,
Cocaine,
4-Acetoxy-DIPT 200.00 USD Gm
5-MeO AMT 120.00 USD Gm
5-MeO-DIPT 160.00 USD Gm
DMT 260.00 USD Gm
AMT 125.00 USD Gm
DIPT 150.00 USD Gm
2C-B 250.00 USD Gm
2C-1 240.00 USD Gm
2C-T-2 220.00 USD Gm
MDMA 200.00 USD Gm
MDEA 180.00 USD Gm
DOB 280.00 USD Gm
DOM 175.00 USD Gm
TMA-2 180.00 USD Gm
BZP 180.00 USD Gm
GHB 75.00 USD 150 Gm

They may well be legit and deliver your order of, 3 g LSD25, 14g Cocaine and 7g MDMA (but somehow I doubt it!). A better route for the methylenedioxy compounds would be through a well known supplier like;
http://www.research-chemicals.co.uk
There is always a small offering at EBay, although I have never bought any from there. Has anyone had any experience buying or taking research chemicals?
« Last Edit: January 05, 2010, 12:57:38 AM by Naf1 »

shroomedalice

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Re: The research chemical thread
« Reply #1 on: January 05, 2010, 01:30:32 AM »
that mdpv is news to me and very interesting.

cut that carbonyl off and I think its potency will go right up.

so it would seem that pyrole is the go for our amine groups excellent.

the reason I think this is as you extend the alkyl chain you loose potency.
you also loose potency with a carbonyl on the first carbon.

the pyrole on the second carbon must increase potency.

2,5 methoxy 4 methyl propyl -2- pyrol benzene would be very interesting indeed.

or especially the fly analoges :)

thanx Naf nice one.

that may just be the LSD killer if its flyed.

god Id hate to work with the shit so strong.
« Last Edit: January 05, 2010, 01:33:05 AM by shroomedalice »

Vesp

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Re: The research chemical thread
« Reply #2 on: January 05, 2010, 01:34:09 AM »
Yeah I really like the idea of this thread. Seems helpful. I see a few of these listed on ebay as bonsai research fertilizer. It is funny, and questionable.
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Naf1

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Re: The research chemical thread
« Reply #3 on: January 05, 2010, 02:13:27 AM »
"It is funny, and questionable."

The only questionable thing is the motives of people like us!

Understanding Plants Using Research Chemicals

http://www.thefreelibrary.com/Understanding+Plants+Using+Research+Chemicals-a01074014288

"There has been a lot of research done on plant functions like their growth and understanding the factors affecting them. Serotonin has recently gained immense attention because scientists believe they influence the growth of plants. However there is also a new area of research in this chapter that has come forth and that is the role of specific research chemicals and the influence they have on serotonin and plant growth functions.

Though serotonin is more famous for its wide variety of applications in animals, it has existed in plants long before even the appearance of animals. Thus, serotonin could find a major application in the evolution of life. Serotonin has been suggested to be actively involved in various physiological roles in plants including flowering, morphogenesis and adaptation in response to the changes in the environment. Serotonin also has been found to direct the growth of light capturing structures in plants towards the light source.

Thus, this had led to active research being pursued on trials on mephedrone and methylone and their potential abilities to showcase the effect of serotonin in cultivation and growth of plants. Mephedrone is a complex ketone that is a water soluble compound and is an excellent candidate for research in effect of serotonin on plant growth. Another great option to study research in effect of serotonin on plant growth is to buy methylone as it has similar properties as mephedrone.

Thus plant researchers are desperate to buy methylone and mephedrone so that they can study the experimental plant treatments specifically focused on providing research into the effects of ketones and serotonin in plant growth. Furthermore, it is believed that there are many secrets that one can unlock in understanding the relationships between these research chemicals, serotonin and plants. But a lot of scientists are still in the dark when it comes to the knowledge about the molecular characterization of serotonin's regulatory and functional roles which has spurred them to do increasing research in this area.

However, it is essential that one take notice of important factors to keep in mind before one goes ahead to buy butylone or methylone and mephedrone for research activities. These research chemicals should preferably be provided in pure crystalline powder form and should be of the highest purity. Since there is no specific mephedrone shop from where these chemicals can be bought or information about these compounds can be obtained, one should be aware that these chemicals are not for human consumption and for botanical research purposes only. Hence, one needs to check their national laws before ordering these research chemicals.

Serotonin unquestionably has some important applications in the way it influences the way in which a plant grows. But a lot of focus is now on research chemicals like methylone that can affect serotonin and its control on plant growth as it might lead us to understand our green friends a lot better and in turn learn something about our own evolution."

There would be much more open research like this happening if it were not for the people (like us) abusing the chemicals and taking them like candy. There are videos of young 16 olds on you tube that have eaten like 5g of mephedrone and filming themselves running around like lunatics and it is a big joke(that is disturbing) as there have been numerous deaths from that particular chem. "

Each of the research chemicals, do actually have numerous legitimate research applications!
« Last Edit: January 05, 2010, 03:06:33 AM by Naf1 »

Vesp

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Re: The research chemical thread
« Reply #4 on: January 05, 2010, 03:00:46 AM »
Interesting.. I had no idea, very interesting read - but they are selling them in suspiciously small amounts I do believe. 120 to 450mg, for $$ to $$$ money.
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jon

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Re: The research chemical thread
« Reply #5 on: January 06, 2010, 05:53:37 AM »
funny idea huh? yah know jon's been getting reviews like this from propionoxy loperamide

"it turned out to be a pretty mellow long lasting buzz with analgesia superior to oxycodone.. wow.. worth making again"
hmmm? can't wait to crack that p-chloro nut.
if you think that's good this is 40 fold better

Naf1

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Re: The research chemical thread
« Reply #6 on: January 07, 2010, 01:38:53 AM »
"if you think that's good this is 40 fold better"

The only thing is I am not an opiate lover, dont get me wrong some codeine and a few bowls and I am happy. But I am not really into the tranquilizers, analgesics, barbiturates etc. I would much rather a couple of points of mephedrone any day, I would have preferred meth but in my older days am leaning towards the methylenedioxyphenyl compounds. Mephedrone would be about as speedy as I would get nowadays! Plus giving birth to a two pound turd after a couple of days on imodium is enough to make me not want to do that!


Naf1

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Re: The research chemical thread
« Reply #7 on: January 07, 2010, 05:04:37 AM »
It would have to mentioned that Methylone could be reduced to a secondary alcohol with sodium borohydride or using the method from below;

Hydrogen transfer reduction of ketones using formic acid as a hydrogen donor under hydrothermal conditions

Zheng SHEN, Fang-ming JIN†‡, Ya-lei ZHANG, Bing WU, Jiang-lin CAO

Abstract

The hydrothermal experiments with ketones and formic acid showed that the hydrogen transfer reduction of ketones
can be conducted using formic acid as a hydride donor in the presence of NaOH at 300 °C. The yield of alcohols was considerably
higher at a much lower ratio of hydrogen source to ketones than the traditional Meerwein-Ponndorf-Verley (MPV) reduction,
reaching 60% for isopropanol from acetone and 70% for lactic acid from pyruvic acid. Water molecules may act as a catalyst in the
hydrogen transfer reduction of ketones under hydrothermal conditions.

http://www.springerlink.com/content/808ut4835450n345/

The secondary alcohol could then be reduced to MDMA by the usual suspects (Birch, RP etc). If Butylone was bought and treated the same way, one would end up with MDEA. Also 4-Aco-DMT could be subjected to simple hydrolysis to afford 4-hydroxy-DMT (psilocin 4-HO-DMT) which could be taken as is or for example treated with hydrobromic acid to afford 4-bromo-DMT which could be used as a starting material for lysergic acid for example. It could be used as a protecting group while condensing it with isocinchomeronic acid it could be subjected to a N-dealkylation used for tertiary amines after the fact. There would be many things one could do with such things ;D

jon

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Re: The research chemical thread
« Reply #8 on: January 07, 2010, 05:13:36 AM »
naf you sure like to complicate things.
300 C huh?
this is incompatable with many organic reactions exept maybe cracking and pyrollysis.
re:
 being stopped up and shitting bowling balls.
all opiates do this you could take hydrocodone 20 mg for ex: and not crap for two days if yu had no tolerance but when you get tolerance you also get your shit together as it were i speak metaphorically and phillosophicaly of course ;D

Naf1

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Re: The research chemical thread
« Reply #9 on: January 07, 2010, 05:19:41 AM »
"naf you sure like to complicate things.
300 C huh?"

Can you provide a more OTC method of reducing ketones to secondary alcohols? Without using sodium borohydride, as I think this would be a handy reaction to have in the tool box if one could do it without the 300*C that was more a theoretical proposal (so any ideas?).

" being stopped up and shitting bowling balls."

Roflmao!

jon

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Re: The research chemical thread
« Reply #10 on: January 07, 2010, 06:40:28 AM »
hmm probably a dissolving metal reduction like al/hg the problem there is that instead of a reduced ketone you get a pinacol dimer.
so i can't really say twat about that meerwin pondorf varley reduction you can use different catalysts besides aluminum isopropoxide i'm not well versed on that scheme but that's practical.

psilocin 4-HO-DMT) which could be taken as is or for example treated with hydrobromic acid to afford 4-bromo-DMT which could be used as a starting material for lysergic acid for example

no i don't think so aromatic sytems react differently that would be akin to me saying well i could react phenol with hydrobromic acid to yeild the aryl bromide it just won't happen.
« Last Edit: January 07, 2010, 09:20:29 AM by jon »

Naf1

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Re: The research chemical thread
« Reply #11 on: January 08, 2010, 01:57:11 AM »
"no i don't think so aromatic sytems react differently that would be akin to me saying well i could react phenol with hydrobromic acid to yeild the aryl bromide it just won't happen."

Oh yeah, I get a bit carried away sometimes (lol).

jon

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Re: The research chemical thread
« Reply #12 on: January 08, 2010, 03:49:30 PM »
i'm very concrete and analytical i don't meander top far off the beaten path i guess we think differently.

Naf1

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Re: The research chemical thread
« Reply #13 on: January 09, 2010, 03:29:15 AM »


Phenyl lactic acid ref;
OXIDATION OF SOME ?-HYDROXY-ACIDS WITH LEAD TETRA-ACETATE
http://www.journalarchive.jst.go.jp/english/jnlabstract_en.php?cdjournal=bcsj1926&cdvol=9&noissue=1&startpage=8

Besides the streochemistry being off, that seems feasible! There is some memory of chirality but the product would be racemic, so any phenylalanine could be used.
« Last Edit: January 09, 2010, 03:37:19 AM by Naf1 »

shroomedalice

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Re: The research chemical thread
« Reply #14 on: January 09, 2010, 03:37:40 AM »
easier going to PAN from phenylalanine then useing that.

I was one of the first to get that to work and it is truly easy though WD is still screaming it is having probs with it.

also if we go through tone we can add the pyrol to it

I have been thinking about that pyrol on the second carbon its cyclic as you know just like oxalone.

this would make me belive that any kind of cyclic amine on the second carbon would be of interest.
couple this with a couple of flys on the benzene ring and still we are getting stronger.

pyrol might not be the strongest either.
« Last Edit: January 09, 2010, 03:46:37 AM by shroomedalice »

Naf1

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Re: The research chemical thread
« Reply #15 on: January 09, 2010, 03:46:12 AM »
Whats PAN?

"I was one of the first to get that to work and it is truly easy though WD is still screaming it is having probs with it."

??? What are we talking about?

I believe that method is completely OTC except for the methyl iodide, all the other reagents are easy to get (swapping Lithium for sodium in the Wurtz reaction).

shroomedalice

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Re: The research chemical thread
« Reply #16 on: January 09, 2010, 03:49:33 AM »
pan is phenyl aceto nitrile or benzylcyanide

from there you got a heap of ways some otc some not.

in grams 1 phenyl 1/2 caustic use some water to disolve then add 1 tcca slowly.
other bases will work too.

Naf1

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Re: The research chemical thread
« Reply #17 on: January 09, 2010, 04:06:16 AM »
"easier going to PAN from phenylalanine then useing that"

Well to each his own I guess, I am going to have to run this one though, all I need is the MeI.

shroomedalice

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Re: The research chemical thread
« Reply #18 on: January 09, 2010, 04:09:22 AM »
go for it man it sound interesting and I am not always about the easy ways.

its got some realy good solid chem in that route and methyl iodide is not hard to make and is very usefull.

best of luck if I can be of any help let me know.

timecube

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Re: The research chemical thread
« Reply #19 on: January 09, 2010, 01:41:46 PM »
I remember there were some problems with halogenating ephedrine due to a rearrangement that occurs afterward.  I'm not sure if that applies here, but it's something to keep in mind if problems arise at that step.

I'm all for trying new routes, but this seems more complicated by miles than the original suggested workup:


phenylalanine -> phenylacetaldehyde

PA + methylamine -> N-methylphenethylimine  (needs to be done with a dean-stark apparatus to remove the water as it forms.  EDIT:  Maybe not, see Method 2 in second link)

N-methylphenethylimine + MeMgI -> L,D-methamphetamine
(previous product would need to be dried thoroughly, MeMgI isn't that hard to make OTC.  I've been considering MeMgBr as a possibility too)

http://www.erowid.org/archive/rhodium/chemistry/p2p.strecker.html
http://www.erowid.org/archive/rhodium/chemistry/meth.phenylacetaldehyde.html


I have been considering a similar route to MDMA via L-DOPA.  Apparently psychokitty had been working on a similar path from methyldopa which would avoid the grignard step, but methyldopa is restricted in my country.

This thread has gone way off topic, though, and the second half probably needs split off and moved to Drug Synthesis?
« Last Edit: January 09, 2010, 01:50:47 PM by timecube »