돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236467생성일: 2026년 10월 26일

L-Alanine → Boc-Gly-Ala-OH

https://huagongshe.com/reaction/236467

반응식

참여 물질

역할이름HCID투입량
반응물L-AlanineHCID 5950—
반응물TriethylamineHCID 8471—
반응물N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
반응물N-HydroxysuccinimideHCID 80170—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물Boc-Gly-Ala-OHHCID 1112859041.5%

반응 단계

Boc-Gly-Ala-OH was prepared by an N-hydroxysuccinimide coupling procedure. Boc-Gly-OSu (7.67 g, 28.2 mmol) was dissolved in 10 mL of dimethylsulfoxide and the resulting solution was added to a solution consisting of H-Ala-OH (3.76 g, 42.3 mmol) and triethylamine (5.89 mL, 42.3 mmol) in 20 mL of water. After stirring overnight, a precipitate was removed by filtration. The remaining solution was diluted with water and then acidified with hydrochloric acid. An aqueous phase separated from which product was extracted by addition of ethyl acetate. The ethyl acetate extract was washed with 0.2N hydrochloric acid and then saturated sodium chloride prepared in 0.2N hydrochloric acid. The washed ethyl acetate solution was then dried over sodium sulfate and filtered. Solvent was then evaporated, leaving a foamy product, which was crystallized from ethyl acetate:hexane to yield 2.88 g of Boc-Gly-Ala-OH (m.p. 128°-130°).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04644055
출처 데이터셋uspto-grants-1987_02
ORD IDord-5f4e8b8470144a09bcc9d74752d34e24
출처 메모uspto-grants-1987_02