December 27, 2024, 03:38:42 PM
Forum Rules: Read This Before Posting


Topic: Selective reducing agent. Nitro to amine.  (Read 20301 times)

0 Members and 1 Guest are viewing this topic.

Offline OC pro

  • Chemist
  • Full Member
  • *
  • Posts: 396
  • Mole Snacks: +36/-15
  • Gender: Male
Re: Selective reducing agent. Nitro to amine.
« Reply #15 on: July 24, 2010, 09:30:34 AM »
It doesn´t matter if it stinks. All the matter is if the reaction works  ;D.
But I agree...organosulfur chemistry is a bit painful. I was running reactions with Lawesson´s reagent on a several hundred grams scale last week. My technician who had to conduct the experiments was a bit pissed... 8)

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Selective reducing agent. Nitro to amine.
« Reply #16 on: August 28, 2010, 02:55:47 AM »
Use mild hydrogenation, azide to amine. Be aware the system you generate will be a redox system, that is the N-oxide can move between the two nitrogen atoms, so you will end up with a mixture of N-oxides

Development Chemists do it on Scale, Research Chemists just do it!
My Research History


Sponsored Links