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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45475생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 2-(Benzyloxy)-3-tert-butyl-3'-(1-(2-methoxyphenyl)vinyl)biphenyl

https://huagongshe.com/ko/reaction/45475

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물1-(2'-(Benzyloxy)-3'-tert-butylbiphenyl-3-yl)-1-(2-methoxyphenyl)ethanolHCID 58238599—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(Benzyloxy)-3-tert-butyl-3'-(1-(2-methoxyphenyl)vinyl)biphenylHCID 5823857678%

반응 단계

A solution of crude 37 (2.23 mmol) in toluene (80 mL) was treated with p-toluenesulfonic acid (100 mg) and refluxed under a Dean-Stark trap for 3 hr. After cooling, the reaction mixture was diluted with ethyl acetate (150 mL) and washed with saturated sodium bicarbonate (150 mL) and water (2×100 mL). The organic extract was dried over sodium sulfate and filtered. The solvent was removed in a rotary evaporator and the crude product was purified by chromatography on silica (75 g) with 2% ethyl acetate in heptane (4 L) to afford 38 (0.78 g, 78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541522B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-62a6c106885c494f8622bda6f18f757d
출처 메모uspto-grants-2013_09