Chlorotrimethylsilane as a mild and effective source of acid catalyst in reductive benzylation

Minoru Izumi, Koichi Fukase

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

New reductive benzylation of hydroxy functions was effected by using the combination of benzaldehyde, TMSCl, and Et3SiH. TMSCl first reacts with alcohols to form HCl, which is probably the ultimate catalyst for this reaction system. TMSCl can also trap water and thus effectively promote dehydration reactions when more than stoichiometric amount of TMSCl is used. Although excess TMSCl was required for the foregoing reactions, TMSCl could be readily removed by simple evaporation.

Original languageEnglish
Pages (from-to)594-595
Number of pages2
JournalChemistry Letters
Volume34
Issue number4
DOIs
Publication statusPublished - Apr 5 2005

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Dehydration
Evaporation
Alcohols
Catalysts
Acids
Water
trimethylchlorosilane
benzaldehyde

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Chlorotrimethylsilane as a mild and effective source of acid catalyst in reductive benzylation. / Izumi, Minoru; Fukase, Koichi.

In: Chemistry Letters, Vol. 34, No. 4, 05.04.2005, p. 594-595.

Research output: Contribution to journalArticle

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