Reaction of benzene solutions of arylacetylenes with 1 equiv. of chloroacetone and 2 equiv. of Et3N, using a mixture of (PPh3)4 Pd and CuJ as catalyst, affords 1,4-diaryl-butadiynes in very good yields. Under similar reaction conditions aliphatic 1-alkynes yield mixtures of simmetrically disubstituted 1,4-dialkyl-1,3-butadiynes and of 3-alkyl-4-(1-alkynyl)-hexa-1,5-diyn-3-enes.

A palladium-promoted route to 3-alkyl-4-(1-alkynyl)hexa-1,5-dyn-3-enes and/or 1,3-diynes

ROSSI, RENZO;CARPITA, ADRIANO;
1985

Abstract

Reaction of benzene solutions of arylacetylenes with 1 equiv. of chloroacetone and 2 equiv. of Et3N, using a mixture of (PPh3)4 Pd and CuJ as catalyst, affords 1,4-diaryl-butadiynes in very good yields. Under similar reaction conditions aliphatic 1-alkynes yield mixtures of simmetrically disubstituted 1,4-dialkyl-1,3-butadiynes and of 3-alkyl-4-(1-alkynyl)-hexa-1,5-diyn-3-enes.
Rossi, Renzo; Carpita, Adriano; Bigelli, C.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11568/3337
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