Issue 0, 1967

Naturally-occurring thiophens. Part IV. Synthesis of some 2,2′-bithienyl derivatives from cuprous acetylides

Abstract

The synthesis of 5-(but-3-en-1-ynyl)-, 5-(but-3-en-1-ynyl)-5′-methyl-, 5-(but-3-en-1-ynyl)-5′-methoxycarbonyl-, 5-(but-3-en-1-ynyl)-5′-hydroxymethyl-, 5-(4-hydroxybut-1-ynyl)-, 5-(prop-1-ynyl)-, 5-(3-formylprop-1-ynyl)-, 5-(3-hydroxyprop-1-ynyl)- and 5-(3-oxobut-1-ynyl)-2,2′-bithienyl from appropriate cuprous acetylides is described.

The reactions of 5-iodo-2,2′-bithienyl with cuprous cyanide or thiocyanate to give 5-cyano-2,2′-bithienyl and with cuprous acetate to give 2,2′:5′,2″:5″,2′″-quaterthienyl are included. 2,2-Bithienyl and the 5,5′-dimethyl derivative were prepared from the corresponding Grignard reagents by reaction with cobaltous chloride and the same method was used for 2,2′-bifuran. Some derivatives of this system are described.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 2011-2015

Naturally-occurring thiophens. Part IV. Synthesis of some 2,2′-bithienyl derivatives from cuprous acetylides

R. E. Atkinson, R. F. Curtis and G. T. Phillips, J. Chem. Soc. C, 1967, 2011 DOI: 10.1039/J39670002011

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