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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27350생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 4-(2-Furyl)-2-butanone

https://huagongshe.com/reaction/27350

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Methyl vinyl ketoneHCID 6570—
반응물FuranHCID 8029—
생성물4-(2-Furyl)-2-butanoneHCID 1278067%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221713
출처 데이터셋uspto-grants-1980_09
ORD IDord-950327fa9df74ad2a319295d4f309b30
출처 메모uspto-grants-1980_09