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p-Toluenesulfonic acid → 4-(2-Furyl)-2-butanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Methyl vinyl ketone | HCID 6570 | — |
| 反応物 | Furan | HCID 8029 | — |
| 生成物 | 4-(2-Furyl)-2-butanone | HCID 12780 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04221713 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-950327fa9df74ad2a319295d4f309b30 |
| 出典メモ | uspto-grants-1980_09 |