HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 345565Erstellt: 24. Oktober 2026
Diethyl Ether → alpha-(4-Fluorophenyl)-1,2-benzenedimethanol
https://huagongshe.com/de/reaction/345565
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-(4-Fluorobenzoyl)benzoic acid | HCID 82099 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | alpha-(4-Fluorophenyl)-1,2-benzenedimethanol | HCID 14230258 | — |
Reaktionsschritte
To 1190 parts of 1,1'-oxybisethane were added at once 50 parts of lithium aluminium hydride. Then there was added dropwise a solution of 213.7 parts of 2-(4-fluorobenzoyl)benzoic acid in 875 parts of 1,1'-oxybixethane so that the mixture was kept at reflux temperature. Upon completion, stirring was continued first for 30 minutes at room temperature, then for 2 hours at reflux and further overnight at room temperature. The reaction mixture was cooled to 0° C. and there were added dropwise successively 50 parts of water, 50 parts of a 15% sodium hydroxide solution and 150 parts of water all at 0° C. The reaction mixture was filtered over Hyflo and washed thoroughly with 1,1'-oxybisethane. The organic phase was separated, washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of benzene and hexane, yielding 170.4 parts of α-(4-fluorophenyl)-1,2-benzenedimethanol; mp. ±75° C. (intermediate 91).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05057525 |
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| Quelldatensatz | uspto-grants-1991_10 |
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| ORD ID | ord-83002c2fecf54737a80502cb8ef1e28a |
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| Quellennotiz | uspto-grants-1991_10 |
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