Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70257생성일: 2026년 10월 25일
Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamide
https://huagongshe.com/reaction/70257
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) | HCID 6639 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 반응물 | Ethyl 5-(4-hydroxyphenyl)-2-thiophene carboxylate | HCID 58276533 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-{4-[(2-Chloroethyl)oxy]phenyl}-2-thiophenecarboxamide | HCID 58276468 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822518B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-3e2683c486124a4c96c2957d818c48fc |
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| 출처 메모 | uspto-grants-2014_09 |
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