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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565288생성일: 2026년 10월 24일

Potassium Carbonate → 2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/565288

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
반응물BromoisopreneHCID 53976308—
용매AcetoneHCID 180—
생성물2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl esterHCID 11759197—

반응 단계

To a stirred solution of (4-methoxy-benzenesulfonyl)-acetic acid ethyl ester (5.16 g, 20 mmol), isoprenyl bromide (3.0 g, 20 mmol) and 18-Crown-6 (500 mg) in acetone (250 ml) was added K2CO3 (10 gms, excess) and the mixture refluxed foe 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% ethy acetate: hexane. The product 2-(4-methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester was isolated as a colourless oil. Yield: 3.0 g, 93%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06172057B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-38c567a749204ef4915213ea3d8356c1
출처 메모uspto-grants-2001_01