Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560117생성일: 2026년 10월 26일
Benzenesulfonyl chloride → 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide
https://huagongshe.com/reaction/560117
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Benzenesulfonyl chloride | HCID 7369 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Potassium bisulfate | HCID 516920 | — |
| 반응물 | 2-[2-(3-bromo-phenyl)-2-hydroxy-ethylamino]-N-phenyl-acetamide | HCID 67000657 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide | HCID 67001090 | 99% |
반응 단계
To a cooled suspension of 2-[2-(3-bromo-phenyl)-2-hydroxy-ethylamino]-N-phenyl-acetamide (840 mg) and N,N-diisopropylethylamine (760 mL) in methylene chloride (20 mL) was added benzenesulfonyl chloride (0.31 mL). The mixture was stirred at 0° C. for 1 hour and at room temperature overnight. A 1M aqueous solution of KHSO4 was added, the phases were separated, and the inorganic one was extracted with ethyl acetate (×2). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, n-heptanelethyl acetate 1:1) to yield 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide (1.17 g, 99%) as a white foam, MS: 489.0 (M+H, 1Br)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08063088B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-a8fa243c783a4b308a853d399fde4904 |
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| 출처 메모 | uspto-grants-2011_11 |
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