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HRID 70257作成日:2026年10月26日
Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamide
https://huagongshe.com/reaction/70257
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) | HCID 6639 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Trimethylaluminum | HCID 16682925 | — |
| 反応物 | Ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylate | HCID 58276533 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamide | HCID 58276468 | — |
反応手順
To a suspension of ammonium chloride (2.12 g, 39.6 mmol) in 10 ml of toluene at 5° C. was added dropwise 19.8 ml of 2M trimethylaluminum in toluene solution. The mixture was stirred for 2 h at the room temperature and ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylate (Intermediate KK-1-1) (1.98 g, 7.03 mmol) was added. The resulting mixture was heated at 55-60° C. for 15 h, cooled to 5° C. and quenched with ethanol (10 ml). All solvents were removed in vacuo and the residue was treated with 80 ml of 0.5M HCl solution. A yellow solid was collected by filtration, washed with water and air-dried (1.64 g). The product was added to a mixture of 2-chloroethyl p-toluenesulfonate (4.07 ml, 22.5 mmol) and potassium carbonate (3.11 g, 22.5 mmol) in 100 ml of acetonitrile. After heating at reflux for 40 h, the reaction mixture was filtered to remove the solids, concentrated to dryness in vacuo and purified by silica gel column chromatography using Hexanes and EtOAc to give the title compound as a light yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08822518B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-3e2683c486124a4c96c2957d818c48fc |
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| 出典メモ | uspto-grants-2014_09 |
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