1416470-23-9Relevant articles and documents
Deamination of 3-(dialkylamino)-1,4-diarylhex-5-en-1-ynes during vacuum distillation
Chukhajian,Shahkhatuni,Chukhajian, El. O.,Ayrapetyan,Panosyan
, p. 178 - 183 (2017)
During vacuum distillation of 3-(dialkylamino) derivatives of 1,4-diphenyl- and 4-phenyl-1-(p-chlorophenyl) hex-5-en-1-ynes deamination occurs resulting in a high yield of p-diarylbenzenes. The amines transformation into terbenzenes is a domino-reaction: first step consists in the β-elimination of secondary amines with the generation of conjugated dienyne which via an electrocyclic reaction transforms into cyclic allene intermediate. The latter after 1,3- or 1,5-hydride shift quickly converts into the final reaction products.