Author Topic: MMDA-2 precursor from pepper  (Read 1407 times)

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3base

  • Guest
MMDA-2 precursor from pepper
« on: June 05, 2002, 09:06:00 AM »
piperine can be isolated from pepper and converted to piperic acid.

over 130 years ago (!) in 1869 fittig mielck described very detailed
[1](page 47-56) the cleavage of piperic acid to a compund they called
mono-bromo-piperonal. they wrote: "the preparation of this compund is
extremely easy and we obtained it each time in considerable quantity ..."

they used for the simple preparation: bromine, Na2CO3 and alcohol.

furthermore they performed extensive investigations on this compund,
beside other results, they found that mono-bromo-piperonal is extremely
easy volatile with steam, insoluble in cold water and sparsely in boiling
water. it crystallizes from alcohol in long, bendable and completely
colorless and glittery needles and melts at 129°C to a colorless liquid.
the molecular formula is C8H5BrO3.

[1]  analen der chemie und pharmacie, 1869 152, 25-58
     "untersuchungen ueber die constitution des piperins
     und seiner spaltproducte piperinsaeure und piperidin"
     rud fittig, w h mielck

in the paper are no particulars about the structure of mono-bromo-piperonal.
but piperonal has only 3 possible positions for a ring substitution
with bromine. so lets see what the internet nowadays knows about this
compund:

   6-bromo-piperonal
   =================
   Molecular Formula: C8H5BrO3
   Molecular Weight: 229.03
   CAS Number: 15930-53-7
   Air sensitive, Store under nitrogen
   Melting Point (°C): 128 to 132

   6-BROMO-1,3-BENZODIOXOLE-5-CARBOXALDEHYDE
   =========================================
   Molecular Formula: C8H5BrO3
   CAS Number: 15930-53-7

[

http://www.sigmaaldrich.com/

]



[

http://www.interchim.com/interchim/chemical/combinatorial_chemistry/hetero/otherheterocycles5.htm

]

BINGO !!!  :)

so it looks like mono-bromo-piperonal and 6-bromo-piperonal
are the same.

and 6-bromo-piperonal again is a precursor for:

MMDA-2

(http://www.erowid.org/library/books_online/pihkal/pihkal133.shtml)

Nemo_Tenetur

  • Guest
very good finding!
« Reply #1 on: June 06, 2002, 04:57:00 AM »
This should be rated as "excellent"!
Easy, high yielding sythesis. A valuable precursor for some NOT-SCHEDULED analogs (at least here in Germany!).

Rhodium

  • Guest
3base: You don't have access to the actual paper ...
« Reply #2 on: June 06, 2002, 06:28:00 AM »
3base: You don't have access to the paper in question so that the actual procedure can be had?

Antoncho

  • Guest
Steam-distillables.
« Reply #3 on: June 06, 2002, 09:43:00 AM »
Absolutely cool, 3base! I mean, fucking excellent! You made my day :)

So..... now we have a fully functional 'piperine routeset' analogous to the one that already exists for vanillin ;D
At least, we will have it if the bromination procedure is found in explicit form ;)

Only you,  naturally, will 1st have to isolate piperine from pepper - but that's easy.

Another interesting mooment - they say bromopiperonal is very easy to steam-distill; makes me kinda wonder if the same rule would also apply to bromo-p-DMB :)




Antoncho

moo

  • Guest
6-bromopiperonal from piperic acid
« Reply #4 on: October 08, 2002, 11:59:00 AM »
Here it is, someone please translate it.

Annalen der Chemie und Pharmacie 152, 25-58 (1869):

Die Darstellung dieser Verbindung ist aufserordentlich leicht, wenn
man auf die oben beschriebene Weise 1 Mol. Piperinsäure mit 2 bis 3 Mol.
Brom zusammenbringt, das product in heifsem Alkohol löst, nach dem Erkalten
die abgeschiedene Piperinsäure abfiltrirt, darauf den Alkohol verdunstet
und den harzigen Rückstand mit kohlensaurem Natrium und Wasser so lange
destillirt, bis sich im Kühlrohr keine Krystalle mehr verdichten. Die so
erhaltene Verbindung ist nahezu rein. Um sie vollständiger zu reinigen kann
man sie nochmals mit Wasser destilliren oder aus siedendem Alkohol oder
Benzol umkrystallisiren.
            Die Analyse ergab für diese Verbindung die Formel C8H5BrO3. Sie ist
demnach Monobrompiperonal.
           Das Monobrompiperonal ist unlöslich in kaltem, etwas löslich in
siedendem Wasser, leicht löslich in heifsem alkohol, wenig löslich in kaltem.
Aus Alkohol krystallisirt es in langen, biegsamen, völlig farblosen und
glänzenden Nadeln. Aus siedendem Benzol, worin es leicht löslich ist, wurde
es in harten Tafeln erhalten. Es schmilzt bei 129° zu einer farblosen
Flüssigkeit, erstarrt wieder krystallinisch und verflüchtigt sich schon bei
70° merklich. Mit Wasserdämpfen ist die reine Verbindung so leicht flüchtig,
dafs sich enge Kühlröhren in sehr kurzer Zeit verstopfen.




Rhodium

  • Guest
Translation
« Reply #5 on: October 08, 2002, 12:35:00 PM »
2-3 moles of bromine is added to piperic acid in the manner described above, the product recrystallized from alcohol and after cooling the precipitated unreacted piperic acid is filtered off and the alcohol is evaporated to give a resin, which is distilled together with aqueous sodium carbonate until no more crystals are deposited in the condenser. The product is relatively pure, but can be purified further by another steam distillation or recrystallization from alcohol or benzene.

The product 6-bromopiperonal is insoluble in cold water, somewhat soluble in boiling water, very soluble in boiling alcohol, not much in cold alcohol. The compound crystallizes from alcohol in long, shiny colorless needles. The melting point is 129°C.

No1CockSucker

  • Guest
P#19
« Reply #6 on: October 13, 2002, 02:05:00 PM »
6-bromo-MDX is a rough ride from what I understand.

Kind of like T#19 I would suppose.

As for N-X-(2-Me0)-4,5-MDO-Amp, I believe Ann used the phrase, 'not the smoothest of drugs.'

However, I can only describe 2-MeO-3,4-MDO-Amp as "extremely uplifting" [in my own words].  Luckily, I found some acid that night and that kept me from getting too "high."

catastrophe

  • Guest
moo please help!
« Reply #7 on: December 09, 2002, 03:23:00 PM »

2-3 moles of bromine is added to piperic acid in the manner described above




Moo, if you still have the ref. what is the bromination procedure "described above"? SWIM assumes that it is conducted in alcohol, probably methanol, correct? SWIM wants to verify because brominating in haloalkanes leads to tetrabromopiperic acid according to 3-base's page. Thanks.


moo

  • Guest
Oops
« Reply #8 on: December 09, 2002, 04:20:00 PM »
It's a good thing someone noticed that one. I'm sick of typing up something in a language I have trouble understanding even with the help of a dictionary and will scan the whole article.

Rhodium

  • Guest
Fittig Article
« Reply #9 on: December 09, 2002, 07:28:00 PM »

catastrophe

  • Guest
Thanks
« Reply #10 on: December 11, 2002, 11:11:00 AM »
Thanks very much!