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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1275249생성일: 2026년 10월 26일

2-Cyclopenten-1-one → ethyl (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/reaction/1275249

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyclopenten-1-oneHCID 13588—
반응물(2-Ethoxy-2-oxoethyl)dimethylsulphonium bromideHCID 78861—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Hydrochloridesodium chlorideHCID 19796930—
용매TolueneHCID 1140—
생성물ethyl (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 1072577668.3%

반응 단계

A suspension of carboethoxymethyl dimethylsulfonium bromide (45.5 g, 198.6 mmol) in toluene (350mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g, 198.4 mmol). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g, 238.4 mmol). After an additional 18 hours, the reaction mixture was added to a 1 N hydrochloric acid/sodium chloride solution. The resulting mixture was extracted with diethyl ether. The combined ether extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified using silica-gel chromatography, eluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes, to give 22.81 g (68%) of the title compound. Melting point: 36-38° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06160009
출처 데이터셋uspto-grants-2000_12
ORD IDord-a99dddab673340a385d556171f8ffed8
출처 메모uspto-grants-2000_12