A mild and efficient procedure for the preparation of acid chlorides from carboxylic acids

Doo Ok Jang; Doo Jin Park; Kim Joonggon

doi:10.1016/S0040-4039(99)00967-3

A mild and efficient procedure for the preparation of acid chlorides from carboxylic acids

Doo Ok Jang, Doo Jin Park, Kim Joonggon

Chemistry and Medical Chemistry

Research output: Contribution to journal › Article › peer-review

87 Citations (Scopus)

Abstract

Various carboxylic acids are converted into the corresponding acid chlorides by treatment with trichloroacetonitrile and triphenylphosphine in methylene chloride at room temperature. Aryl acids show higher reactivity than alkyl acids under the conditions.

Original language	English
Pages (from-to)	5323-5326
Number of pages	4
Journal	Tetrahedron Letters
Volume	40
Issue number	29
DOIs	https://doi.org/10.1016/S0040-4039(99)00967-3
Publication status	Published - 1999 Jul 16

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(99)00967-3

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title = "A mild and efficient procedure for the preparation of acid chlorides from carboxylic acids",

abstract = "Various carboxylic acids are converted into the corresponding acid chlorides by treatment with trichloroacetonitrile and triphenylphosphine in methylene chloride at room temperature. Aryl acids show higher reactivity than alkyl acids under the conditions.",

author = "Jang, {Doo Ok} and Park, {Doo Jin} and Kim Joonggon",

year = "1999",

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T1 - A mild and efficient procedure for the preparation of acid chlorides from carboxylic acids

AU - Jang, Doo Ok

AU - Park, Doo Jin

AU - Joonggon, Kim

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Y1 - 1999/7/16

N2 - Various carboxylic acids are converted into the corresponding acid chlorides by treatment with trichloroacetonitrile and triphenylphosphine in methylene chloride at room temperature. Aryl acids show higher reactivity than alkyl acids under the conditions.

AB - Various carboxylic acids are converted into the corresponding acid chlorides by treatment with trichloroacetonitrile and triphenylphosphine in methylene chloride at room temperature. Aryl acids show higher reactivity than alkyl acids under the conditions.

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U2 - 10.1016/S0040-4039(99)00967-3

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VL - 40

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EP - 5326

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 29

ER -

A mild and efficient procedure for the preparation of acid chlorides from carboxylic acids

Abstract

All Science Journal Classification (ASJC) codes

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