HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64648Erstellt: 25. Oktober 2026
1,2-Dibromoethane → 2-[2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenoxy]-ethyl bromide
https://huagongshe.com/reaction/64648
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dibromoethane | HCID 7839 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenol | HCID 13672174 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-[2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenoxy]-ethyl bromide | HCID 13672175 | 58,4% |
Reaktionsschritte
To an ethanol solution of sodium ethylate obtained by dissolving 0.7 g of metallic sodium in 50 ml of ethanol were added 8.9 g of 2,6-dichloro-4-(2,2,2-trifluoroethylthio)-phenol and 20 g of ethylene bromide. The mixture was stirred at 40° C. for 2 hours and under reflux for 4 hours. Ethanol and the excess of ethylene bromide were evaporated. The residue was taken into 150 ml of toluene, washed with a 5% aqueous solution of potassium hydroxide and water in this sequence, and dried over anhydrous sodium sulfate. Toluene was evaporated, and the residue was distilled under reduced pressure to give 7.2 g of 2-[2,6-dichloro-4-(2,2,2-trifluoroethylthio)-phenoxy]-ethyl bromide with the b.p.=124°-126° C./0.8 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-ea7863179ebd4bd8baa5658f7a499e8f |
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| Quellennotiz | uspto-grants-1986_09 |
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