Convenient preparation of tert-butyl β-(protected amino)esters

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Abstract

Refluxing an aldehyde 1 with benzotriazole and benzylcarbamate in the presence of a catalytic amount of p-TsOH gave the corresponding benzyloxycarbonylamino-1-(1-benzotriazolyl)alkane 2 in good yields. Compounds 2 treated with substituted tert-butyl acetates 3 using LDA as a base afford smoothly and under mild conditions the N-2-protected 3-aminoalkanoic esters 4.

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Katritzky, A. R., Kirichenko, K., Elsayed, A. M., Ji, Y., Fang, Y., & Steel, P. J. (2002). Convenient preparation of tert-butyl β-(protected amino)esters. Journal of Organic Chemistry, 67(14), 4957–4959. https://doi.org/10.1021/jo0110810

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