600538411
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Methylenedioxy 4MAR... Possible?
Could one perform an akabori on piperonal to yield MD-PPA then further take this to an MD-4MAR equiv. with sodium cyanate?
With the extended activity of 4MAR, this seems like it could be one interesting phenethylamine...
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joe_aldehyde
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haha...UTFSE  i asked that a while ago. sandmeyer said that methoxy-substituted
phenyloxazolines have decreased activity compared to the unsubstituted one.
but what about p-fluorophenyl-oxazoline...
ah and forget about akabori, it seems like no one that attempted it ever got something useful out of it, strange enough. condense the aldehyde with
nitroethane in presence of a tertiary (alkanol)amine.
[Edited on 13-9-2005 by joe_aldehyde]
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Kinetic
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Europhoric analogues
| Quote: | | sandmeyer said that methoxy-substituted phenyloxazolines have decreased activity compared to the unsubstituted one. |
No he didn't: https://sciencemadness.org/talk/viewthread.php?tid=4343
Para-fluoro-4-methylaminorex is not really worth making either. I made it a couple of years ago from 4-fluoropropiophenone. Bandil posted a bioassay
of his 4-fluoro-4-MAR at the Hive a couple of years ago too. His synthesis can be found here: http://www.erowid.org/archive/rhodium/chemistry/para-fluoro-...
My experience was a little better than his, but it was not interesting enough to warrant making it again. There are certainly more interesting things
to focus on. I still wonder what 4-ethylaminorex will be like.
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joe_aldehyde
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oh...my apologies, kinetic!
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