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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35713생성일: 2026년 10월 23일

Triethylamine → N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl ester

https://huagongshe.com/ko/reaction/35713

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Tert-butoxycarbonylalanineHCID 85082—
반응물D-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 2802425—
용매DichloromethaneHCID 6344—
생성물N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl esterHCID 13369188—

반응 단계

To a solution of 23.0 g. (0.121 m) of N-t-butoxycarbonyl-L-alanine, 42.6 g. (0.121 m) of D-alanine benzyl ester p-toluenesulfonic acid salt and 17 ml. (0.121 m) of triethylamine in 400 ml. of cold (0° C.) methylene chloride was added dropwise 25.0 g. (0.121 m) of dicyclohexylcarbodiimide in 100 ml. of methylene chloride. After stirring overnight at room temperature the solids were filtered and the filtrate concentrated to an oil. The residue was dissolved in 400 ml. of ethyl acetate which was washed with a 1% hydrochloric acid solution, a 10% potassium carbonate solution, water and a brine solution. The organic phase was separated, dried over magnesium sulfate and concentrated to an oil. The residue was triturated with diethyl ether and the resulting solids filtered under nitrogen, 16.0 g. An additional 12.7 g. of the desired product crystallized from the filtrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767743
출처 데이터셋uspto-grants-1988_08
ORD IDord-8a2f92c2d143402187baa2f3871614ad
출처 메모uspto-grants-1988_08