56523-74-1Relevant academic research and scientific papers
ACTION DU CHLORURE D'ACETYLE ET DE L'ANHYDRIDE ACETIQUE SUR LE NITRONATE DE LITHIUM DERIVE DU PHENYL-2 NITROETHANE. REACTIVITE ELECTROPHILE OU DIPOLAIRE, EN FONCTION DU MILIEU, DE L'OXYDE DE NITRILE INTERMEDIAIREMENT FORME
Cherest, M.,Lusinchi, X
, p. 3825 - 3840 (2007/10/02)
The lithium nitronate salt derived from 2-phenyl nitroethane reacts with acetic anhydride and with acetyl chloride to give an intermediate nitrile oxide.Depending on the protonating character of the medium, this latter can react either as a 1,3 dipole to give the furoxan or, in the presence of a dipolarophile, the corresponding adduct; or as an electrophile leading to the chlorooxime or to derivatives of benzohydroxamic acid.The formation of the nitrile oxide, by loss of acetic acid from a nitronic-acetic mixed anhydride, appears to be the most plausible reaction pathway accounting for the above observations.
SUR LA TRANSFORMATION DU β-NITROSTYRENE SOUS L'ACTION DU CHLORURE D'ACETYLE EN PRESENCE D'UN CHLORURE METALLIQUE
Guillaumel, Jean,Demerseman, Pierre,Clavel, Jean-Marc,Royer, Rene,Platzer, Nicole,et al.
, p. 2459 - 2465 (2007/10/02)
While β-nitrostyrene yields only hydroxymic or hydroxamic acid derivatives by treatment with acetyl chloride in the presence of zinc, tin, titanium or aluminium chloride, it also gives 3-chloro-2-indolinone and a 5-acetyl derivative of the latter, when th
