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HRID 375595作成日:2026年10月24日

Ethyl Acetate → Hexahydro-2-oxo-4-(5-phenyl-3-oxo-1E-pentenyl)-cyclopenta[b]furan

https://huagongshe.com/ja/reaction/375595

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium HydroxideHCID 14798—
反応物Dimethyl(2-oxo-4-phenylbutyl)phosphonateHCID 2733973—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒DichloromethaneHCID 6344—
生成物Hexahydro-2-oxo-4-(5-phenyl-3-oxo-1E-pentenyl)-cyclopenta[b]furanHCID 18993488—

反応手順

To a solution of dimethyl(2-oxo-4-phenylbutyl)phosphonate (1.40 g, 5.46 mmol), [3aα,4β,5α]-hexahydro-2-oxo-cyclopenta[b]furan-4-carboxaldehyde (4) (0.765 mg, 4.96 mmol) and triethylbenzyl ammonium chloride (110 mg 0.48 mmol) in dichloromethane (10 mL) at room temperature was added a 10M aqueous solution sodium hydroxide (0.55 mL, 5.5 mmol) and the resulting mixture was vigorously stirred for 40 min. The reaction was then diluted with ethyl acetate and washed with water (2×10 mL) and brine (1×10 mL) and concentrated in vacuo. Column chromatography (1:2 ethyl acetate-hexanes through silica gel) provided the title compound 5 as a clear, colorless oil (1.29 g, 4.53 mmol). Rf =0.42 in ethyl acetate-hexanes, 1:1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05486540
出典データセットuspto-grants-1996_01
ORD IDord-ab4c9de3c96148dba114727323ef4fb6
出典メモuspto-grants-1996_01