Reaction of sec-amides with metal hydride. II. Reaction of acid chlorides with sodium acetanilidoborohydride.

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Abstract

Sodium acetanilidoborohydride prepared from acetanilide and sodium borohydride in α-picoline reduced acid chlorides to alcohols in dichloromethane. On the other hand, this reducing reagent prepared in pyridine did not reduce acid chlorides but reduced the pyridine ring to give acylpiperidines.

Journal

  • Chemical and Pharmaceutical Bulletin

    Chemical and Pharmaceutical Bulletin 24(8), 1939-1943, 1976

    The Pharmaceutical Society of Japan

Codes

  • NII Article ID (NAID)
    110003635204
  • NII NACSIS-CAT ID (NCID)
    AA00602100
  • Text Lang
    ENG
  • ISSN
    0009-2363
  • Data Source
    NII-ELS  J-STAGE 
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