Protected amino acid tetrafluorophenyl esters for peptide synthesis

New 2,3,5,6‐tetrafluorophenyl active esters of protected amino acids useful for peptide synthesis were prepared in high yield. For certain amino acid derivatives such as Boc‐Pro‐OH, Boc‐Ile‐OH, and Boc‐Val‐OH, their tetrafluorophenyl esters have significantly higher melting points than the corresponding pentafluorophenyl esters. Kinetic studies were carried out to compare the racemization rate constants (with triethylamine) and coupling rate constants (with valine methyl ester) of the tetrafluorophenyl and pentafluorophenyl esters of protected histidine and tyrosine. Results of the second‐order kinetics showed similarly large k coupling /k racemization ratios for both tetra‐ and pentafluorophenyl esters. In particular, the use of 2,3,5,6‐tetrafluorophenyl or pentafluorophenyl ester prevents extensive racemization of the N‐tert. ‐butyloxycarbonyl‐ N im ‐benzyl‐histidine.