戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 359357作成日:2026年10月25日

Sodium Hydroxide → 2,2-Dimethyl-5-[2-(4-fluorophenyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/359357

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物4-FluorobenzaldehydeHCID 68023—
反応物3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Sodium ChlorideHCID 5234—
生成物2,2-Dimethyl-5-[2-(4-fluorophenyl)ethenyl]-3(2H)-furanoneHCID 5450358260.1%

反応条件

温度50 °C

反応手順

To a solution of 2,2,5-trimethyl-3(2H)-furanone (2.0 g, 15.9 mM) and 4-fluorobenzaldehyde (1.6 g, 13.2 mM) in ethanol (100 mL), was added 1N aqueous sodium hydroxide (1.6 mL, 1.6 mM). The reaction solution was heated at 50° C. for four hours. After the reaction solution was cooled to room temperature and diluted with saturated aqueous sodium chloride (200 mL) and water (200 mL), the aqueous solution was extracted with diethyl ether (2×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (25 mL), dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford a dark yellow crystalline solid. The crude product was recrystallized from hexane to give light yellow crystals (1.8 g, 45% yield), m.p. 55°-57° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05001126
出典データセットuspto-grants-1991_03
ORD IDord-f7c4370264ef4afa9c17b83d3ff7a798
出典メモuspto-grants-1991_03