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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922생성일: 2026년 10월 23일

1,2-Dichloroethane → N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester

https://huagongshe.com/ko/reaction/1922

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Allyl AlcoholHCID 7858—
반응물Ethyl AcetateHCID 8857—
반응물(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl EsterHCID 53793486—

반응 단계

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726319
출처 데이터셋uspto-grants-1998_03
ORD IDord-36f08b8e5c0c4222ab2cf761a8e66449
출처 메모uspto-grants-1998_03