Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → (RS)-2-(2-buten-1-yl)-6-methoxy-1-indanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 2,2-Dimethoxypropane | HCID 6495 | — |
| 반응물 | 3-Buten-2-ol | HCID 11716 | — |
| 반응물 | 6-Methoxy-1-Indanone | HCID 334036 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (RS)-2-(2-buten-1-yl)-6-methoxy-1-indanone | HCID 54031441 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05646173 |
| 출처 데이터셋 | uspto-grants-1997_07 |
| ORD ID | ord-e1496153e2bd4337af31d50f11c970cb |
| 출처 메모 | uspto-grants-1997_07 |