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    Author(s): Peter E. Laks; Richard W. Hemingway
    Date: 1987
    Source: Journal of the Chemical Society Perkin Trans. I. 465-470
    Publication Series: Miscellaneous Publication
    PDF: View PDF  (2.1 MB)


    Reaction of polymeric procyanidins (condensed tannins) with toluene-α-thiol at pH 12.0 and 23°C gave predominantly one stereoisomer of 1.3-bisbenzylthio-1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl) propan-2-ol (10) by stereoselective reaction at C-4 and C-2 of the Quinone methide derived from the upper 2,3-cis procyanidin units. Smaller amounts of two isomers of 1-benzylthio-1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl)propan-2-ol (4) were obtained by reaction at the C-2 of catechin obtained from the terminal units. At higher temperatures, (10) loses toluene-α-thiol preferentially from C-1 to give 1-benzylthio-1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl)- propan-2-one (11) by a tautomeric rearrangement of the Quinone methide via an enol to the ketone. Loss of toluene-α-thiol from (4) gave 1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl)propan-2-one (5) by a similar rearrangement. This compound further rearranges to 1-(3,4-dihydroxyphenyl)-4,6-dihydroxyindan-2-one (6).

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    Laks, Peter E.; Hemingway, Richard W. 1987. Condensed tannins: Base-catalysed reactions of polymeric procyanidins with toluene-α-thiol, liability of the interflavanoid bond and pyran ring. Journal of the Chemical Society Perkin Trans. I. 465-470

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