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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565283생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
용매AcetoneHCID 180—
생성물2-(4-Methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl esterHCID 10893429—

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06172057B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-6beca1c808a5402799974d9739ed08a9
출처 메모uspto-grants-2001_01