HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 560117Erstellt: 25. Oktober 2026
Benzenesulfonyl chloride → 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide
https://huagongshe.com/reaction/560117
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Potassium bisulfate | HCID 516920 | — |
| Edukt | 2-[2-(3-bromo-phenyl)-2-hydroxy-ethylamino]-N-phenyl-acetamide | HCID 67000657 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-{benzenesulfonyl-[2-(3-bromo-phenyl)-2-hydroxy-ethyl]-amino}-N-phenyl-acetamide | HCID 67001090 | 99% |
Reaktionsschritte
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)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08063088B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-a8fa243c783a4b308a853d399fde4904 |
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| Quellennotiz | uspto-grants-2011_11 |
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