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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274025생성일: 2026년 10월 27일

Benzeneacetic acid, 3,4-dimethoxy-, methyl ester → alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester

https://huagongshe.com/reaction/274025

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneacetic acid, 3,4-dimethoxy-, methyl esterHCID 85213—
반응물SodiumHCID 5360545—
반응물2,3-dihydro-6-methoxy-1H-isoindol-5-olHCID 10241135—
반응물(5-Bromopentyl)(1,1-dimethylethyl)dimethyl silaneHCID 19042078—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl esterHCID 54212729—

반응 조건

온도-78 °C

반응 단계

To a solution, -78° C. under argon, of 2 38 g of 3,4-dimethoxyphenyl acetic acid methyl ester in 30 ml of tetrahydrofuran is added 12.45 ml of 1.0M sodium hexamethylsidilazide. The solution is stirred at -78° C. for 5 minutes and then warmed to 0° C. for 1 hour. To this solution is added 3.5 g of (5-bromopentyl)(1,1-dimethylethyl)dimethyl silane. The reaction mixture is allowed to warm to room temperature and stirred for 12 hours. The mixture is diluted with diethyl ether and water, the layers are separated and the organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: hexane/ethyl acetate,5/1) to give 2.6 g of the desired product as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387685
출처 데이터셋uspto-grants-1995_02
ORD IDord-278b8b799112408cad48b628991a6464
출처 메모uspto-grants-1995_02