4.7 Article

Synthesis of α-Hydroxy Carboxylic Acids via a Nickel(II)-Catalyzed Hydrogen Transfer Process

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 353, Issue 11-12, Pages 1918-1922

Publisher

WILEY-BLACKWELL
DOI: 10.1002/adsc.201100241

Keywords

hydrogen transfer process; alpha-hydroxy carboxylic acids; lactic acid; nickel-catalyzed reaction; primary alcohols

Funding

  1. National Science Council, Taiwan [NSC-96-2113M-007-020MY3]
  2. Fujian, China [2009HZ0004-1]

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A new catalytic system for beta-alkylation of lactic acid with primary alcohols has been developed. In the presence of nickel(II) acetate tetrahydrate [Ni(OAc)(2)(H(2)O)(4)] and base, lactic acid reacts with primary alcohols to afford the corresponding coupled alpha-hydroxy carboxylic acids in good to excellent yields via a hydrogen transfer process without any hydrogen acceptor or hydrogen donor.

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