The Hive > Tryptamine Chemistry
AMT -> AET?
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synesthesia:
I'm almost 100% sure that you can't but.. Is there any possibility of converting AMT(a-MethylTryptamine) to AET(a-EthylTryptamine?
synesthesia:
Thought so :) Brain farts just happen ;) Do you know of any substitue for LAH?
It's fun programming your quantum computer!
psyloxy:
I don't know of a direct substitute for LAH. But there is almost always an alternatice synthetic way. Think of the nitrostyrene reduction: Shulgin uses LAH all the time. but you can also do it with [NaBH4 + NiCl2] or electrolytically or first reduce the double bond with NaBH4, then the nitro group. Or you could go the phenylethanol --> phenylethyl-iodid --> PEA way... this is what I love about organic chemistry.
--psyloxy--
synesthesia:
Yeh I just see DET. But it doesn't mean that it isn't illegal (I don't know Canadian laws that much).. They might have an analogue act?
http://canada.justice.gc.ca/FTP/EN/Laws/Chap/C/C-38.8.txt
"When I was young I played with legos. But now I am older and I play with atoms."
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