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HRID 43316생성일: 2026년 10월 23일

Potassium Hydroxide → 4-(Tetrahydrofuran-3-yl)-3-buten-2-one

https://huagongshe.com/ko/reaction/43316

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Dimethyl (2-oxopropyl)phosphonateHCID 77872—
반응물3-Furancarboxaldehyde, tetrahydro-HCID 157568—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물4-(Tetrahydrofuran-3-yl)-3-buten-2-oneHCID 67177193—

반응 단계

Dimethyl (2-oxopropyl)phosphonate (32.06 g, 193 mmol) is added to a chilled (ice-bath) solution of potassium hydroxide (10.83 g, 193 mmol) in water (30 ml) and ethanol (170 ml) and the mixture is stirred. Tetrahydrofuran-3-carboxaldehyde (50% wt. % solution in water, 25 ml, 138 mmol) is added dropwise and the reaction mixture is stirred at 5° C. for 10 minutes. The cooling bath is removed and the mixture is stirred at room temperature for 7 hours. Most of the solvent is removed in vacuo, water (100 ml) and diethyl ether (200 ml) are added, the mixture is poured into a separating funnel and the organic phase collected. The aqueous phase is extracted three times with diethyl ether, and the organic extracts are combined, dried over anhydrous magnesium sulphate, filtered and the filtrate is evaporated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate and hexane to give 4-(tetrahydrofuran-3-yl)-3-buten-2-one as a pale yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536351B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cafd4c47a9d24c2c85dda39dc24b23e0
출처 메모uspto-grants-2013_09