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p-Toluenesulfonic acid → 4-Methyl-3-pentylfuran-2(5H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-one | HCID 19801577 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 4-Methyl-3-pentylfuran-2(5H)-one | HCID 15953432 | 77.3% |
反応手順
4-Acetoxy-4-methyl-3-pentyl-tetrahydrofuran-2-one (125.33 g, 549 mmol) is placed with 2.61 g (13.7 mmol) of p-toluenesulphonic acid and held at 150° C. for 4 hours while stirring. The acetic acid which is cleaved off is distilled off over a Vigreux column. The reaction solution, cooled to room temperature, is diluted with 500 ml of ether and washed in a separating funnel with 2×200 ml of sat. NaCl solution. Drying of the ether phase over MgSO4 and concentration on a rotary evaporator as well as distillation at 100°-103° C./0.12 mbar yields 71.34 g (77.3%) of 4-methyl-3-pentyl-2(5H)furanone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05179077 |
| 出典データセット | uspto-grants-1993_01 |
| ORD ID | ord-2aa26145304d413eb1d2861ccb503d06 |
| 出典メモ | uspto-grants-1993_01 |