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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5401생성일: 2026년 10월 24일

Benzyl Bromide → trans Benzyl 3-(acetylthiomethyl)-2-oxo-1-aza-cyclodecane-10-carboxylate

https://huagongshe.com/ko/reaction/5401

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Cesium carbonateHCID 10796—
반응물trans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acidHCID 86747202—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물trans Benzyl 3-(acetylthiomethyl)-2-oxo-1-aza-cyclodecane-10-carboxylateHCID 131718122—

반응 단계

Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid (0.15 g, 0.52 mmol) is dissolved in dimethylformamide (2.5 mL). Benzyl bromide (0.062 mL, 0.52 mmol) and cesium carbonate (0.085 g, 0.26 mmol) are added, and the reaction is stirred at room temperature overnight. The reaction is diluted with water, and the aqueous layer is extracted several times with methylene chloride. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give trans benzyl 3-(acetylthiomethyl)-2-oxo-1-aza-cyclodecane-10-carboxylate m.p. 117°-118° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244889
출처 데이터셋uspto-grants-1993_09
ORD IDord-ee7debe1bbd340b6a45aa36abc48f31c
출처 메모uspto-grants-1993_09