HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248752Erstellt: 24. Oktober 2026
Pyridine → 4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acid
https://huagongshe.com/de/reaction/248752
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Fluoro-3-(trifluoromethyl)aniline | HCID 75377 | — |
| Edukt | 4-(Chlorosulfonyl)benzoic acid | HCID 82385 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acid | HCID 3699990 | — |
Reaktionsschritte
10 g (55.8 mmol) of 4-fluoro-3-trifluoromethylaniline and 6 ml (74.3 mmol) of pyridine are dissolved in 250 ml of dichloromethane. The mixture is cooled with ice water and, under agitation and exclusion of moisture, 12.7 g (57.6 mmol) of 4-chlorosulfonylbenzoic acid is added in incremental portions. The mixture is stirred overnight; the slurry is combined with 75 ml of 2N sodium hydroxide solution, and the organic phase is separated. The alkaline solution is washed with dichloromethane and then adjusted to pH 2 with hydrochloric acid. The product is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulfate and concentrated to dryness. The title compounds melts at 243-°245° C. after crystallization from ethanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05210290 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-b639f8a2c482415fbde171d119d57f67 |
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| Quellennotiz | uspto-grants-1993_05 |
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