21615-25-8Relevant academic research and scientific papers
The reaction of phthalidylidene dichloride with primary amines. Synthesis and X-ray molecular structure of N-substituted phthalisoimides
Guirado, Antonio,Zapata, Andres,Ramirez De Arellano, M. Carmen
, p. 5305 - 5324 (2007/10/03)
An efficient method for the synthesis of N-substituted phthalisoimides, by reaction of phthalidylidene dichloride with primary amines, is described. The reactions with arylamines, arylenediamincs and alkylenediamines lead to the corresponding phthalisoimides or bisphthalisoimides in nearly quantitative yields. However, the reactions with alkylamines are not useful because of the relatively high nucleophilicity of alkylamines. Certain particular behaviours of arylamines, associated with the presence of specific ortho-substituents have been found. The reactions of arylamines bearing an o-hydroxymethyl group provide a convenient method for preparing 2-benzoxazinylbenzoic acids. The X-ray crystallographic structures of N-(2-methoxyphenyl)phthalisoimide 3a and 2-(4H-3.1-benzoxazin-2-yl)benzoic acid 15a have been determined.
FEATURES OF THE REACTION OF PHTHALOYL CHLORIDE WITH PRIMARY AMINES
Ganin, E. V.,Makarov, V. F.,Rozynov, B. V.
, p. 1772 - 1777 (2007/10/02)
The reaction of phthaloyl chloride with primary amines, which leads to the formation of the N,N'-substituted diamides of phthalic acid, takes place through the intermediate formation of the N-substituted isophthalimides.The reactivity of these compounds i
