Issue 21, 1972

Rearrangement of benzylidenecarbene formed by pyrolysis of the benzylidene derivative of meldrum's acid at 560°

Abstract

Flash-vacuum pyrolysis of the benzylidene compound (2) gives acetone and phenylacetylene (98%); 13C labelling shows that the presumed intermediate benzylidenecarbene (3) appears to undergo 75% of hydrogen migration and 25% of phenyl migration at 560°.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1175-1175

Rearrangement of benzylidenecarbene formed by pyrolysis of the benzylidene derivative of meldrum's acid at 560°

R. F. C. Brown and K. J. Harrington, J. Chem. Soc., Chem. Commun., 1972, 1175 DOI: 10.1039/C39720001175

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