Like most of my threads this starts off with some guy (nomud) on Wetdreams says...
Starting from p-xylene, by distilling commercial xylenes.p-xylene distills over first fraction by 1 degree C less than m-xylene.p-xylene is about 18-20% of commercial m,o,p-xylenes.Luckily, this fraction will crystallize in a stoppered flask in the freezer,in an hour or two,pour off any remaining liquid and recryst.repeat,redistill,repeat for 99% p-xylene.Figure swiy's mole eq. wt. and proceed to bromination of ring with mole eq. Br2 and pinch of iron powder as cat,or possibly Br2 in AcOH [in dark].For monoBromo p-xylene.Then a Friedel Crafts propionylation w/ either propionic acid,or anhydride or propionyl chloride, swiy's choice of cats. and reagents.To yield the 4-Br 2,5-dimethyl propiophenone.The alpha carbon-ketone halogenation is done w/ chlorine water.Then methylamineate to title substance.Mephedrone seems to have some toxicity,likely due to the mono-paramethyl group,as does p-methoxyamphetamine.This should be smoother and less toxic,more potent.And almost as easy a synth..Swim will likely test on pet gorilla next month
http://www.drugs-forum.com/forum/showthread.php?t=93427
So 4-Bromo 2,5-dimethylpropiophenone is that right? Can I also get a paper on carbon-ketone halogenation? Is it just halonating a ketone with a carbon bond? Also why can you use regular propionic acid instead of propionyl chloride? I don't know what that is so I am having trouble visualizing this whole reaction. My current guess is...
2C8H10+Br2--->2C8H9Br+H2
C8H9Br+C3H6O2--->C11H13BrO+H2O
And here is my big question mark.
C11H13BrO+CH5N--->C11H15NO+CH3Br
I also drew a pretty picture
Starting from p-xylene, by distilling commercial xylenes.p-xylene distills over first fraction by 1 degree C less than m-xylene.p-xylene is about 18-20% of commercial m,o,p-xylenes.Luckily, this fraction will crystallize in a stoppered flask in the freezer,in an hour or two,pour off any remaining liquid and recryst.repeat,redistill,repeat for 99% p-xylene.Figure swiy's mole eq. wt. and proceed to bromination of ring with mole eq. Br2 and pinch of iron powder as cat,or possibly Br2 in AcOH [in dark].For monoBromo p-xylene.Then a Friedel Crafts propionylation w/ either propionic acid,or anhydride or propionyl chloride, swiy's choice of cats. and reagents.To yield the 4-Br 2,5-dimethyl propiophenone.The alpha carbon-ketone halogenation is done w/ chlorine water.Then methylamineate to title substance.Mephedrone seems to have some toxicity,likely due to the mono-paramethyl group,as does p-methoxyamphetamine.This should be smoother and less toxic,more potent.And almost as easy a synth..Swim will likely test on pet gorilla next month
http://www.drugs-forum.com/forum/showthread.php?t=93427
So 4-Bromo 2,5-dimethylpropiophenone is that right? Can I also get a paper on carbon-ketone halogenation? Is it just halonating a ketone with a carbon bond? Also why can you use regular propionic acid instead of propionyl chloride? I don't know what that is so I am having trouble visualizing this whole reaction. My current guess is...
2C8H10+Br2--->2C8H9Br+H2
C8H9Br+C3H6O2--->C11H13BrO+H2O
And here is my big question mark.
C11H13BrO+CH5N--->C11H15NO+CH3Br
I also drew a pretty picture