Oxidative coupling of malononitrile with formation of 1,1,2,3,3-pentacyanopropene salts
✍ Scribed by Vladimir A. Kaminskii; Oleg Yu. Slabko; Andrey V. Kachanov; Boris V. Buhvetskii
- Book ID
- 104252620
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 92 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A simple and convenient route for the synthesis of 1,1,2,3,3-pentacyanopropene salts is reported. These salts are formed by interaction of malononitrile with SeO 2 in presence of organic N-containing bases or pyridinium salts.
📜 SIMILAR VOLUMES
## Abstract Treatment of 3‐(2,4‐dimethoxyphenylamino)‐ and 3‐methylamino‐1‐phenylbut‐2‐en‐1‐ones with some benzenediazonium tetrafluoroborates gives, besides the usual azo coupling products [i.e., 3‐(substituted imino)‐1‐phenylbutane‐1,2‐diones 2‐(4‐substituted phenylhydrazones) and 2‐(4‐methoxyphe