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HRID 43316作成日:2026年10月23日

Potassium Hydroxide → HCID 67177193、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Dimethyl (2-oxopropyl)phosphonateHCID 77872—
反応物3-Furancarboxaldehyde, tetrahydro-HCID 157568—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物HCID 67177193HCID 67177193—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536351B2
出典データセットuspto-grants-2013_09
ORD IDord-cafd4c47a9d24c2c85dda39dc24b23e0
出典メモuspto-grants-2013_09