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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5393생성일: 2026년 10월 24일

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/ko/reaction/5393

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
반응물HCID 178418680HCID 178418680—
용매Diethyl EtherHCID 3283—
생성물Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930812—

반응 조건

온도0 °C

반응 단계

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (5.02 g, 20.81 mmol) is dissolved in ether (50 mL), and cooled to 0° C. Trimethylsilylmethylmagnesium chloride (42.0 mL of a 1.0M solution in ether, 42.0 mmol) is added dropwise, the reaction is stirred at 0° C. for 20 minutes, and then heated to reflux overnight. The reaction is quenched with saturated ammonium chloride, and extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate; major isomer, m.p. 129°-130° C.; minor isomer, m.p. 175°-177° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244889
출처 데이터셋uspto-grants-1993_09
ORD IDord-d4fb9e46ad954be7a349fa818cd8a137
출처 메모uspto-grants-1993_09