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HRID 238172作成日:2026年10月26日

Water → Tert-butyl 3-methyl-2-(4-methylphenyl)pentanoate

https://huagongshe.com/reaction/238172

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-BromobutaneHCID 6554—
反応物tert-Butyl (4-methylphenyl)acetateHCID 12362014—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 3-methyl-2-(4-methylphenyl)pentanoateHCID 58074556—

反応条件

温度0 °C

反応手順

Under argon, 19.58 g (174.5 mmol) of potassium tert-butoxide were initially charged in 200 ml of DMF, the mixture was cooled to 0° C., 30 g (145.4 mmol) of tert-butyl (4-methylphenyl)acetate, dissolved in 50 ml of DMF, were added slowly and the mixture was then stirred at 0° C. for 30 min. 18.95 ml (174.5 mmol) of 2-bromobutane were then slowly added drowise, and the solution was stirred at 0° C. for 4 h. 200 ml of water and 200 ml of diethyl ether were then added to the reaction solution. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were dried over magnesium sulfate. After filtration, the solvent was removed under reduced pressure. The crude product was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 20:1). This gave 15.5 g (59.1 mmol, 40.6% of theory) of a colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642592B2
出典データセットuspto-grants-2014_02
ORD IDord-d849c72962184e80be70b139d94a6ff1
出典メモuspto-grants-2014_02