How does this work so? is this not on a secondary hailed?
xxxxx
- Larvae
- Posts: 8
jon
- Foundress Queen
- Posts: 1,883
yeah the stickig point is always making that solution it's not easy took me a good 6 months until i got it down to a science.
lots of trial and error.
lots of trial and error.
Wizard X
- Lord of the Realms
- Foundress Queen
- Posts: 1,224
How does this work so? is this not on a secondary hailed?
http://en.wikipedia.org/wiki/Del%C3%A9pine_reaction
http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv5p0121
CH3-X =[Delépine reaction]=> CH3-NH2
jon
- Foundress Queen
- Posts: 1,883
it works but it takes a good month.
i was reading the only exception of it working on a secondary halide was isopropyl iodide and that very SLOWLY.
i was reading the only exception of it working on a secondary halide was isopropyl iodide and that very SLOWLY.
xxxxx
- Larvae
- Posts: 8
Would http://www.erowid.org/archive/rhodium/chemistry/dmmda-2.html not be the same type of reaction. It claims to transform iododillapiole to DMMDA-2 using the Delpine reaction.
I don't see any references so is that just people talking shit?
Quote
Extraction of iodosafrole left to your own imagination. Our trade secret!!
Finally, amination is done at room temp with methylamine for MDMA or with
hexamine (via Delepine process) to get MDA or other analog.
Happy trails! Pugsley and Wednesday.
http://www.erowid.org/archive/rhodium/chemistry/halosafrole.txt
I don't see any references so is that just people talking shit?
jon
- Foundress Queen
- Posts: 1,883
yeah that is (people talking shit)
i used to have the refernces to back up what i'm talking about, isopropyl iodide was an 'exception' it does react delepine style but it takes a month to do so.
proove it wrong.
i noticed the author has a tendancy to make outrageous claims if you read his writtings.
i used to have the refernces to back up what i'm talking about, isopropyl iodide was an 'exception' it does react delepine style but it takes a month to do so.
proove it wrong.
i noticed the author has a tendancy to make outrageous claims if you read his writtings.
Wizard X
- Lord of the Realms
- Foundress Queen
- Posts: 1,224
Would http://www.erowid.org/archive/rhodium/chemistry/dmmda-2.html not be the same type of reaction. It claims to transform iododillapiole to DMMDA-2 using the Delpine reaction.QuoteExtraction of iodosafrole left to your own imagination. Our trade secret!!
Finally, amination is done at room temp with methylamine for MDMA or with
hexamine (via Delepine process) to get MDA or other analog.
Happy trails! Pugsley and Wednesday.
http://www.erowid.org/archive/rhodium/chemistry/halosafrole.txt
I don't see any references so is that just people talking shit?
http://www.organic-chemistry.org/namedreactions/delepine-reaction.shtm
Mechanism of the Delépine Reaction: An SN2 reaction leads to the hexamethylentetramine salt. In chloroform, the starting materials are soluble whereas the products crystallize out.
Palladium: Dissolve your pure iodosafrole and hexamethylentetramine in chloroform and stopper well with a glass stopper. If a reaction occurs over time, the iodosafrole hexamethylentetramine salt product will crystallize out.
This is the simplest reaction test.
atara
- Dominant Queen
- Posts: 256
You could use cyanate anion as a nucleophile to attack the halosafrole forming safrole isocyanate which hydrolyses to MDA. Perhaps?
jon
- Foundress Queen
- Posts: 1,883
i don't think it is a strong enough nucleophile.
akcom
- Dominant Queen
- Posts: 430
I'd be pretty surprised if a cyanate couldnt replace a halide (esp. iodine). But that's all theoretical. Exp. is king.
igotthere
- Pupae
- Posts: 61
Hi everyone, I'm bumping this post as, in a weeks time, I'll have the best part of a week of evenings plus a whole day to myself and I would like to have another good go at this.
Take a look at my newly started thread - Jon's route.
igt
Take a look at my newly started thread - Jon's route.
igt