So iv been eyeing this compound for a while now (Ariadne) or other related 4C compounds.
I found some nitropropane, well, somewhere to get it at a reasonable price, has anyone done any chemistry in this area?
I have experience with other more standard phenethylamine’s and amphetamine’s and I wonder if it’s much harder or different to that area…
The experience reports of the 4C compounds look interesting.
Is it likely to be a similar case to the 2c and Dox compounds in that, people tend to use the 2,5-DMOaldehyde before adding anything to the 4 position, make the nitrostyrene and then reduce and THEN do the halogination? Where as with the alkylation, it seems people add the alkyl group to the 4 position to the disunited aldehyde first and then proceed with the Henry and reduce.
I hope that makes sense…it does in my head but words I am not good with words.
Anyway yeah if anyone has looked into this in more depth than me please chime in coz it sounds like a cool project.
I found some nitropropane, well, somewhere to get it at a reasonable price, has anyone done any chemistry in this area?
I have experience with other more standard phenethylamine’s and amphetamine’s and I wonder if it’s much harder or different to that area…
The experience reports of the 4C compounds look interesting.
Is it likely to be a similar case to the 2c and Dox compounds in that, people tend to use the 2,5-DMOaldehyde before adding anything to the 4 position, make the nitrostyrene and then reduce and THEN do the halogination? Where as with the alkylation, it seems people add the alkyl group to the 4 position to the disunited aldehyde first and then proceed with the Henry and reduce.
I hope that makes sense…it does in my head but words I am not good with words.
Anyway yeah if anyone has looked into this in more depth than me please chime in coz it sounds like a cool project.