I am looking to synthesize isonicotinic acid from citrazinic acid. The route to get 2,6-dichloro-pyridine-4 carboxilic acid was easy, but the
reduction of halogen need a cheap procedure. (no hydrazine and LiAlH) A little bit of preliminary googling I found this:
What is your opinion about this things
Attachment: php6AuIoN (32kB) This file has been downloaded 697 times
Weinreb - 10-4-2014 at 10:33
I have performed the Mg/isopropyl alcohol reduction on chlorobenzene, yield was excellent on this substrate. The magnesium was standard turnings used
for Grignard reactions. Aqua-regia - 10-4-2014 at 23:46
Thank you, its sounds good. I hope that the pyridine ring don't occurse barrier, or formed dipyridine bond and no spherical inhibition.Dr.Bob - 11-4-2014 at 07:19
