関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4-Dimethylfuran | HCID 19462 | — |
| 反応物 | Acetic acid, 2,2-dichloro-, 1,1'-anhydride | HCID 77772 | — |
| 反応物 | 4-(2-Thienyl)Butyric Acid | HCID 78386 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | 2-[4-(2-Thienyl)butyryl]3,5-dimethylfuran | HCID 19745237 | 90% |
反応手順
In 50 ml of dichloroethane were dissolved 8.51 g (0.05 mole) of 4-(2-thienyl)butyric acid and 14.39 g (0.06 mole) of dichloroacetic anhydride. To the resulting solution was added 0.065 mole of 3,5-dimethylfuran and 0.71 g of boron trifluoride-diethyl ether complex and the resulting mixture was then stirred at 50° C. for 7 hours. After completion of the reaction, the reaction solution was cooled and washed successively with 5% aqueous sodium carbonate solution and water. The organic layer was concentrated under reduced pressure to obtain 2-[4-(2-thienyl)butyryl]3,5-dimethylfuran.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05235068 |
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| 出典データセット | uspto-grants-1993_08 |
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| ORD ID | ord-b193a9e606e44f6099d3fdb5674a580b |
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| 出典メモ | uspto-grants-1993_08 |
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