A convenient procedure for parallel ester hydrolysis
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作者:
Anderson, MO
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机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Anderson, MO
Moser, J
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机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Moser, J
Sherrill, J
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机构:Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Sherrill, J
Guy, RK
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Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Guy, RK
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机构:
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94142 USA
The treatment of alkyl esters with barium hydroxide octahydrate in methanol followed by protonation with anhydrous hydrogen chloride affords carboxylic acids. The procedure does not require aqueous workup and is particularly suitable for parallel synthesis applications.