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HRID 483015作成日:2026年10月26日

Phenethyl bromide → Ethyl 3-oxo-2-(2-phenylethyl)butanoate

https://huagongshe.com/reaction/483015

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物Ethyl AcetoacetateHCID 8868—
反応物Sodium MethoxideHCID 10942334—
溶媒EthanolHCID 702—
生成物Ethyl 3-oxo-2-(2-phenylethyl)butanoateHCID 21945991.3%

反応手順

Ethyl acetoacetate (53.8 g., 0.29 mole) was dissolved in 110 ml. of anhydrous ethanol. Sodium methoxide (17.3 g., 0.36 mole) was added portionwise to the stirred solution, allowing the temperature to rise to 40°-50°. The mixture was then heated to reflux (80°-82°) and phenethyl bromide (53.8 g., 0.32 mole) added dropwise over 1 hour. Reflux was continued for 20 hours. The reaction mixture was cooled to 30°-35° and filtered over diatomaceous earth with ethanol wash. The combined filtrate and wash were concentrated in vacuo to a pot temperature of 50°, cooled to 25°, diluted with 150 ml. of hexane and 40 ml. of water, acidified to pH 6.5-7.0 with 6N HCl. The hexane layer was separated and washed with 25 ml. of fresh water. The aqueous layer were combined and back-washed with 40 ml. of fresh hexane. The hexane layers were combined, washed with 60 ml. of water, dried over 15 g. MgSO4, filtered and evaporated to yield title product as an oil (62 g., 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04576964
出典データセットuspto-grants-1986_03
ORD IDord-273244fa72cc45449396d994d0ae100d
出典メモuspto-grants-1986_03