化工社化工社 化学情報印刷レポート · 研究参考用
Furan → 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Furan | HCID 8029 | — |
| 反応物 | Trifluoroacetic anhydride | HCID 9845 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 6-Methoxycarbonyl-1-carboxy-3-hexyne | HCID 10976151 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne | HCID 11020812 | 92% |
反応手順
To a mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (27.6 g, 0.15 mole), furan (30.7 g, 0.45 mole) and dichloromethane (150 ml) is added trifluoroacetic anhydride (37.8 g, 0.18 mole) at room temperature, and the mixture is reacted at 30°-35° C. for 24 hours. After completion of the reaction, the reaction solution is poured into ice-water and neutralized with 20% aqueous sodium hydroxide solution. The organic layer is separated and washed successively with 5% aqueous sodium hydrogen carbonate solution and water. The organic layer is concentrated under reduced pressure to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (32.3 g, yield; 92%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05191109 |
| 出典データセット | uspto-grants-1993_03 |
| ORD ID | ord-b61e2a66f6604740a7874d7be8fc8165 |
| 出典メモ | uspto-grants-1993_03 |