Gatera, Tharcisse published the artcileOne-Pot, Catalyst-Free Synthesis of Nitriles from Aldehydes Using Aminating Reagent MsONH3OTf, Related Products of nitriles-buliding-blocks, the main research area is nitrile preparation green chem; aldehyde amination.
An eco-friendly protocol to synthesize nitriles RCN (R = naphthalen-2-yl, n-hexyl, 4-bromophenyl, etc.) from their corresponding aromatic and aliphatic aldehydes RCHO in excellent yields has been developed. This is a catalyst-free protocol which employs an aminating reagent (MsONH3OTf) under mild conditions. The hydroxylamine triflic acid salts (MsONH3OTf) acted as the N source for this protocol. The protocol proved to be easy to perform and presented good functional group tolerance.
Synlett published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Related Products of nitriles-buliding-blocks.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts