HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1464565Erstellt: 25. Oktober 2026
Triethylamine → 2-(2-Chloro-2-fluoroethylthio)-phenylsulfonamide
https://huagongshe.com/reaction/1464565
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,2-Dichloro-1-fluoroethane | HCID 79004 | — |
| Edukt | 2-Sulfanylbenzene-1-sulfonamide | HCID 11041532 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2-(2-Chloro-2-fluoroethylthio)-phenylsulfonamide | HCID 19086751 | — |
Reaktionsschritte
A mixture of 217.8 g of the triethylamine salt of 2-mercaptophenylsulfonamide obtained in accordance with Example P6 and 101 g of 1,2-dichloro-1-fluoroethane in 950 ml of methanol is stirred in an autoclave for 24 hours at a temperature of from +65° C. to +70° C. and for a further 24 hours at from +95° C. to +100° C. The reaction mixture is then concentrated by evaporation and the residue is stirred with water. By extracting with ethyl acetate, washing with water, drying over sodium sulfate, concentrating by evaporation and purifying the residue by chromatography with methylene chloride, 99.5 g (49.2% of the theoretical yield) of 2-(2-chloro-2-fluoroethylthio)-phenylsulfonamide having a melting point of from +88° C. to +89° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05306693 |
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| Quelldatensatz | uspto-grants-1994_04 |
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| ORD ID | ord-b03a39ef150a4a4aa23d32bc46f59661 |
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| Quellennotiz | uspto-grants-1994_04 |
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