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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380111생성일: 2026년 10월 26일

Benzoin → (2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidine

https://huagongshe.com/reaction/380111

반응식

참여 물질

역할이름HCID투입량
반응물BenzoinHCID 8400—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-DimethylaminopyridineHCID 21885—
반응물1-benzyl hydrogen (R)-pyrrolidine-1,2-dicarboxylateHCID 111208—
용매DichloromethaneHCID 6344—
생성물(2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidineHCID 54511676—

반응 단계

To a solution of (2R)-N-benzyloxycarbonylproline (5 g) in CH2Cl2 (50 ml) were added benzoin (4.5 g), 1-ethyl 3-(3-dimethylaminopropyl)carbodiimide (3.9 ml), and dimethylaminopyridine (2.6 g) at room temperature under N2. After being stirred for 12 hours at room temperature, the solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3, and brine, dried over MgSO4, and evaporated in vacuo. The obtained compound and CH3COONH4 (8.2 g) were dissolved in acetic acid (50 ml) and the mixture was stirred for 4 hours at 100° C. After the solvent was removed, the residue was partitioned between ethyl acetate and water. The organic layer was washed with water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (2R)-1-benzyloxycarbonyl-2-(4,5-diphenyloxazol-2-yl)pyrrolidine (4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300344B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-286eda49468a416b9cc8faa1d2d8e88a
출처 메모uspto-grants-2001_10