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HRID 462849생성일: 2026년 10월 25일

Triethylamine → N(2,2,4,4-tetramethyltetrahydrothiophene-3-yl)-t-butoxycarbonyl-D-serine amide

https://huagongshe.com/reaction/462849

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물(R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acidHCID 637603—
반응물3-Amino-2,2,4,4-tetramethyltetrahydrothiopheneHCID 13733567—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N(2,2,4,4-tetramethyltetrahydrothiophene-3-yl)-t-butoxycarbonyl-D-serine amideHCID 22824009—

반응 조건

온도-20 °C

반응 단계

To a solution of 2.26 g. (11 mmole) of N-t-butoxycarbonyl-D-serine in 75 ml. of tetrahydrofuran is added 1.47 ml. (10 mmole) of triethylamine and the mixture cooled to -10° C. At this temperature is added 0.96 ml. (10 mmole) of ethyl chloroformate and stirring continued for 15 minutes. After cooling to -20° C., 1.6 g. (10 mmole) of dl-3-amino-2,2,4,4-tetramethyltetrahydrothiophene is added and the resulting mixture is allowed to warm to room temperature. Ethyl acetate is added and the mixture is washed twice with 50 ml. portions of 5% (by weight) aqueous citric acid, aqueous sodium bicarbonate (1×50 ml.) and saturated brine (1×50 ml.). The organic layer is dried (Na2SO4) and evaporated to dryness at reduced pressure to afford N(2,2,4,4-tetramethyltetrahydrothiophene-3-yl)-t-butoxycarbonyl-D-serine amide. This product is used without further purification in the next step. ##STR120##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04517379
출처 데이터셋uspto-grants-1985_05
ORD IDord-cd3b2df9bf8449e3b864b3f8197fb70c
출처 메모uspto-grants-1985_05