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HRID 1275249作成日:2026年10月27日

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

https://huagongshe.com/reaction/1275249

反応式

関与物質

役割名称HCID仕込み量
反応物2-Cyclopenten-1-oneHCID 13588—
反応物(2-Ethoxy-2-oxoethyl)dimethylsulphonium bromideHCID 78861—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Hydrochloridesodium chlorideHCID 19796930—
溶媒TolueneHCID 1140—
生成物ethyl (1S,5R,6S)-2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 1072577668.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06160009
出典データセットuspto-grants-2000_12
ORD IDord-a99dddab673340a385d556171f8ffed8
出典メモuspto-grants-2000_12