関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Clofibric Acid | HCID 2797 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | 2-(4-Chlorophenoxy)-2-methylpropanoyl chloride | HCID 2781312 | — |
反応手順
A mixture of 2-(4-chlorophenoxy)-2-methylpropionic acid (15.0 g) and thionyl chloride (70 ml) was boiled under reflux for 1 hour. The thionyl chloride was distilled off and the residue distilled under vacuum to give 2-(4-chlorophenoxy)-2-methylpropionyl chloride, b.p. 84-87° C. at 0.07 mbar. A solution of this chloride (14.17 g) in dichloromethane (50 ml) was added dropwise to a mixture of 1-(3-aminopropyl)imidazole (7.63 g), triethylamine (6.78 g) and dichloromethane (100 ml) at below 0° C. with stirring. After the addition, the mixtures was allowed to warm up to ambient temperature and stirred at this temperature for 2 hours. Saturated aqueous sodium bicarbonate solution (100 ml) was added and the mixture stirred for 1 hour. The mixture was separated and the aqueous layer was washed with dichloromethane. The combined organic layers were dried and evaporated to give a solid which was recrystallised from ethyl acetate to give 2-(4-chlorophenoxy)-N-[3-(imidazol-1-yl)propyl]-2-methylpropionamide, m.p. 83-84° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06031109 |
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| 出典データセット | uspto-grants-2000_02 |
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| ORD ID | ord-60165454e6c44d4792c7499bd4dac61d |
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| 出典メモ | uspto-grants-2000_02 |
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