The Vespiary
The Hive => Tryptamine Chemistry => Topic started by: Antoncho on December 03, 2000, 01:42:00 AM
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the idea isn't exactly mine but it was undeservedly forgotten anyway
i remember having seen a reference on the hive that stated that refluxing tryptofol with dimethylamine/Raney Ni in alc. soln gives DMT in good yields. no further details were given, but i think that sentence already contains everything one needs exept the rxn time.
Keeping in mind that along with the following facts:
1) Raney Ni is easily made by thermal decomposition of Ni oxalate/ formate
2) tryptofol is only one reduction away from indolylacetic acid (heteroauxin - sodium indolylacetate)
3) heteroauxin is freely available from plant supply stores
4) all other DMT synths require LAH that is so fuckin inaccessible to many of us
, the following obvious questions arise:
1) what of the following reagents can be used for reducing IAA to tryptofol:
a) sodium in EtOH
b) Al isopropoxide
c) Al amalgam
d) tin (II) cloride
2) are there any other simple methods for acid to alcohol reduction?
i sincerely hope that i got some of you bees interested
Antoncho
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i'm intrested but have nothing to offer yet.
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This doesn't quite make sense; where did this idea originate from? What exactly do you mean by 'triptophol'? If its 2-(indole-3-yl)-ethanol, then I seriously doubt it could work that way.
Still, indole acetic acid can readily be used as a starting material for producing DMT. By condensing indole-3-yl-acetic acid with dimethylamine, you have 2-(indole-3-yl)-acetic acid dimethyl amide. If you then reduce the amide, you have DMT. This last reduction can be accomplished using a number of different reducing agents.
But this is certainly not a new idea. This has been used in the literature, and, has been discussed here before.