HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2113161Erstellt: 24. Oktober 2026
Hydrochloric Acid → 1-(4-Benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanol
https://huagongshe.com/de/reaction/2113161
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Edukt | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Edukt | 4-(Benzyloxy)-3-chlorobenzaldehyde | HCID 2735495 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-(4-Benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanol | HCID 69050976 | — |
Reaktionsschritte
To a solution of 4-benzyloxy-3-chlorobenzaldehyde (4.9 g, 20 mmol) and trimethyl(trifluoromethyl)silane (4.4 mL, 30 mmol) in THF (0.10 L) was added a solution tetrabutylammonium fluoride (1.0 M in THF, 2.0 mL). After the reaction was stirred at 25° C. for 3 h, it was acidified with 2 N HCl to pH 2, diluted with ethyl acetate and washed with brine. The organic phase was dried and concentrated and the residue was purified by chramotography on silica gel eluting with 8:2 hexane:ethyl acetate to give 1-(4-benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07524882B2 |
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| Quelldatensatz | uspto-grants-2009_04 |
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| ORD ID | ord-b99b7676da0141c19ba218f3fcf51726 |
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| Quellennotiz | uspto-grants-2009_04 |
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