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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264434생성일: 2026년 10월 27일

p-Toluenesulfonic acid → (RS)-2-(2-buten-1-yl)-6-methoxy-1-indanone

https://huagongshe.com/reaction/264434

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2,2-DimethoxypropaneHCID 6495—
반응물3-Buten-2-olHCID 11716—
반응물6-Methoxy-1-IndanoneHCID 334036—
용매TolueneHCID 1140—
생성물(RS)-2-(2-buten-1-yl)-6-methoxy-1-indanoneHCID 5403144155%

반응 단계

A solution of 20.0 g of 6-methoxy-1-indanone, 31.3 ml of 3-buten-2-ol, 53.5 ml of 2,2-dimethoxypropane and 200 mg of p-toluenesulfonic acid in 200 ml of toluene was brought to boiling. The resulting methanol/acetone mixture was distilled off and the reaction solution was subsequently boiled under reflux overnight. After cooling, the solution was washed with 50 ml of saturated sodium hydrogen carbonate solution. The aqueous washing was extracted with 50 ml of ethyl acetate, the organic phases were combined, dried with magnesium sulfate and evaporated in a vacuum. Purification on silica gel (hexane/diethyl ether 5:1) yielded 13.6 g (55%) of (RS)-2-(2-buten-1-yl)-6-methoxy-1-indanone as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-e1496153e2bd4337af31d50f11c970cb
출처 메모uspto-grants-1997_07