HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64694Erstellt: 23. Oktober 2026
3-(Trifluoromethyl)phenol → 2-Butanol, 4-chloro-1-[3-(trifluoromethyl)phenoxy]-
https://huagongshe.com/de/reaction/64694
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 1,4-Dichloro-2-butanol | HCID 17021 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 2-Butanol, 4-chloro-1-[3-(trifluoromethyl)phenoxy]- | HCID 13120348 | — |
Reaktionsschritte
To a mixture of 0.5 mole (75 g.) of m-trifluoromethylphenol, 1 mole (56 g.) of potassium hydroxide, 100 ml. of water and 400 ml. of isopropanol was added 0.6 mole (84 g.) of 1,4-dichloro-2-butanol with stirring at temperature below 55° C. The resulting reaction mixture was heated at 65° C. for 20 hr., mixed with 2 liters of water, and extracted with 400 ml. of isopropyl ether. The ether extract was washed with 0.5N sodium hydroxide and then with water, dried over sodium sulfate and distilled under reduced pressure. The distillate which was collected at 120°-124° C./0.01 mm. solidified at room temperature and melted at 50°-52° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609735 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-f451d76dd022479d86c4d6ad57a6b1ae |
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| Quellennotiz | uspto-grants-1986_09 |
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