HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64650Erstellt: 25. Oktober 2026
Hydrochloric Acid → 2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenol
https://huagongshe.com/reaction/64650
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,2,2-Trifluoroethyl benzenesulfonate | HCID 296341 | — |
| Edukt | 2,6-Dichloro-4-mercaptophenol | HCID 3016363 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenol | HCID 13672174 | 71,1% |
Reaktionsschritte
64 g of potassium carbonate were added to a solution of 41.9 g of 3,5-dichloro-4-hydroxy-benzenethiol in 200 ml of N,N-dimethylformamide under nitrogen atmosphere. To the stirred mixture were dropped at 30° to 40° C. 55 g of 2,2,2-trifluoroethyl-benzenesulfonate. The whole was stirred at 60° to 70° C. for 6 hours, cooled, mixed with 1.5 l of water, and acidified to pH 2 by dropwise addition of hydrochloric acid. A resulted oil was extracted with toluene and the toluene extract was washed with water. The washed toluene extracted was stirred with 160 ml of a 25% aqueous potassium hydroxide solution, and a water layer was separated. Then the separated water layer was acidified to pH 2 by adding hydrochloric acid. A resulted oil was extracted with toluene. The toluene extract was washed with water, dried over anhydrous sodium sulphate, and evaporated to give a residue. The residue was distilled under reduced pressure to give 42.3 g of 2,6 -dichloro-4-(2,2,2-trifluoroethylthio)-phenol which boiled at 85° to 88° C./1 mmHg.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609669 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-652e40a41dca4bd3b4ebcabd297aa1e2 |
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| Quellennotiz | uspto-grants-1986_09 |
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