Issue 0, 1967

Polypeptides. Part V. The use of t-butyl 2,4,5-trichlorophenyl carbonate in the synthesis of N-t-butoxycarbonyl amino-acids and their 2,4,5-trichlorophenyl esters

Abstract

t-Butyl 2,4,5-trichlorophenyl carbonate, conveniently prepared from phosgene in two stages, reacts cleanly with amino-acids in the presence of bases to give N-t-butoxycarbonyl amino-acids (and 2,4,5-trichlorophenol) in excellent yield. By co-extraction of the N-t-butoxycarbonyl amino-acid and 2,4,5-trichlorophenol from the acidified reaction mixture, followed by treatment of the extracts with NN′-dicyclohexylcarbodi-imide, high yields of the corresponding N-t-butoxycarbonyl amino-acid 2,4,5-trichlorophenyl esters are obtained. These active esters are mostly stable, crystalline solids which may be conveniently used in peptide synthesis.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 2632-2636

Polypeptides. Part V. The use of t-butyl 2,4,5-trichlorophenyl carbonate in the synthesis of N-t-butoxycarbonyl amino-acids and their 2,4,5-trichlorophenyl esters

W. Broadbent, J. S. Morley and B. E. Stone, J. Chem. Soc. C, 1967, 2632 DOI: 10.1039/J39670002632

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