Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → 4-(2-Furyl)-2-butanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Methyl vinyl ketone | HCID 6570 | — |
| 반응물 | Furan | HCID 8029 | — |
| 생성물 | 4-(2-Furyl)-2-butanone | HCID 12780 | 67% |
반응 단계
Methylvinylketone (14 g, 0.2 mol) was added dropwise over a period of about 2 hours to furan (150 ml), containing a trace of p-toluene-sulphonic acid, boiling under reflux. The dark brown reaction mixture was stirred for about 16 hours at room temperature. The excess furan was removed by distillation, after which the residue was distilled under vacuum giving 4-(2-furyl)butan-2-one (18.5 g, 67% yield). In a way analogous to that described in Example II, the ketone was reduced to the corresponding alcohol and subsequently converted to the mesylate (28 g, 92% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04221713 |
| 출처 데이터셋 | uspto-grants-1980_09 |
| ORD ID | ord-950327fa9df74ad2a319295d4f309b30 |
| 출처 메모 | uspto-grants-1980_09 |