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HRID 565283作成日:2026年10月24日

Benzyl Bromide → 2-(4-Methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl ester

https://huagongshe.com/ja/reaction/565283

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
溶媒AcetoneHCID 180—
生成物2-(4-Methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl esterHCID 10893429—

反応手順

To stirred solution of the (4-methoxy-benzenesulfonyl)-acetic acid ethyl ester (2.5 g, 10 mmol), benzyl bromide (1.8 gm, 10 mmol) and 18-Crown-6 (500 mg) in acetone (250 ml) was added K2CO3 (10 gms, excess) and the mixture was refluxed for 24 hours. At the end, the reaction mixture was filtered and the acetone layer was concentrated. The residue obtained was extracted with chloroform, washed well with water, dried over anhydrous MgSO4, filtered and concentrated. The product obtained was purified by silica-gel column chromatography, eluting with 30% ethyl acetate: hexane. The product, 2-(4-methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl ester was isolated as a low melting solid. Yield: 3.0 gm 86%; Low melting solid; MS: 349 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06172057B2
出典データセットuspto-grants-2001_01
ORD IDord-6beca1c808a5402799974d9739ed08a9
出典メモuspto-grants-2001_01