161768-42-9Relevant articles and documents
The facile one-pot synthesis of N-imidoylbenzotriazoles via a Beckmann rearrangement of ketoximes
Pi, Hong-Jun,Liu, Li-Feng,Jiang, Shan-Shan,Du, Wenting,Deng, Wei-Ping
experimental part, p. 6097 - 6100 (2010/09/11)
N-Imidoylbenzotriazoles 2a-m were obtained in good to excellent yields (up to 97%) by the reaction of ketoximes 1a-m with MsCl and subsequently with benzotriazole as a one-pot process in Toluene/CH3CN at reflux temperature via a Beckmann rearrangement.
Microwave-assisted preparations of amidrazones and amidoximes
Katritzky, Alan R.,Khashab, Niveen M.,Kirichenko, Nataliya,Singh, Anamika
, p. 9051 - 9056 (2007/10/03)
(Chemical Equation Presented) In an operationally straightforward and efficient method, amidrazones 1a-h and amidoximes 2a-h are prepared in yields of 65-87% from imidoylbenzotriazoles 3a-h by microwave heating for 5-20 min with the appropriate hydrazine
One-pot synthesis of N-imidoylbenzotriazoles via benzotriazole-mediated Beckmann rearrangement of oximes
Katritzky, Alan R.,Monteux, Daphne A.,Tymoshenko, Dmytro O.
, p. 577 - 578 (2008/02/11)
(Matrix presented) N-Imidoylbenzotriazoles 5a-I are obtained under mild conditions in variable yields (20-87%) by reactions of oximes 2a-I with BtTs 1 via a Beckmann rearrangement.