CONCERNING THE REACTION OF (10-DIAZO-10H-ANTHRACEN-9-YLIDENE)-MALONODINITRILE AND RELATED-COMPOUNDS WITH THE CRYPTOHYDRIDE SYSTEM FORMIC ACID-TRIETHYLAMINE
Af. Vaisburg et al., CONCERNING THE REACTION OF (10-DIAZO-10H-ANTHRACEN-9-YLIDENE)-MALONODINITRILE AND RELATED-COMPOUNDS WITH THE CRYPTOHYDRIDE SYSTEM FORMIC ACID-TRIETHYLAMINE, Monatshefte fuer Chemie, 126(6-7), 1995, pp. 783-788
The reaction of (10-diazo-10H-anthracen-9-ylidene)-malonodinitrile (1)
with the cryptohydride system formic acid - triethylamine was studied
. The reaction product turned out to be anthracen-9-yl-acetonitrile (2
a) instead of the expected 10-dicyanomethyl-9,10-dihydro-anthracene-9-
yl formate. Compounds related to 1 yielded in this reaction the corres
ponding 10-substituted anthracen-9-yl-acetonitriles. A mechanism of th
is reaction is proposed. The product of the formic acid promoted decom
position of 1, compound 3b, as well as its tautomer 4b were also obtai
ned.