戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1765作成日:2026年10月23日

2-Cyclopenten-1-one → Ethyl 2-oxobicyclo[3.1.0]hexane-6-carboxylate

https://huagongshe.com/ja/reaction/1765

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 2-oxobicyclo[3.1.0]hexane-6-carboxylateHCID 56535768.3%

反応手順

A suspension of carboethoxymethyl dimethylsulfonium bromide (45.5 g) in toluene (350 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g). After an additional 18 hours, the reaction mixture was added to a 1N 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 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US05726320
出典データセットuspto-grants-1998_03
ORD IDord-8fef71afc98949c49bc84e25d6876698
出典メモuspto-grants-1998_03