戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 27350作成日:2026年10月27日

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

https://huagongshe.com/reaction/27350

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Methyl vinyl ketoneHCID 6570—
反応物FuranHCID 8029—
生成物4-(2-Furyl)-2-butanoneHCID 1278067%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221713
出典データセットuspto-grants-1980_09
ORD IDord-950327fa9df74ad2a319295d4f309b30
出典メモuspto-grants-1980_09