HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1980398Erstellt: 26. Oktober 2026
Ethyl Bromide → 4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrol
https://huagongshe.com/reaction/1980398
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 4-Fluoro-4'-hydroxybenzophenone | HCID 117666 | — |
| Edukt | Lithium | HCID 3028194 | — |
| Edukt | HCID 178506846 | HCID 178506846 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrol | HCID 14727320 | — |
Reaktionsschritte
To a solution of ethyl lithium prepared from 2.8 g. of lithium metal and 21.8 g. of ethyl bromide in 265 ml. of dry ether a solution of 10.8 g. of 4-fluoro-4'-hydroxy-benzophenone in 50 ml. of dry tetrahydrofurane is added dropwise, with stirring in argon atmosphere, at a temperature between -40° C. and -30° C. When the addition is complete, the mixture is allowed to warm up to 0° C., and is then stirred at this temperature for further 30 minutes. The mixture is decomposed with a 20% aqueous ammonium chloride solution under cooling. The aqueous phase is extracted with ether, the ethereal phases are combined, washed to neutral with water, and dried over anhydrous magnesium sulfate. The solution is evaporated under reduced pressure, and the solid residue is crystallized from a mixture of n-hexane and ethyl acetate to yield 8.2 g. of the named product, melting at 125° to 126° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04508926 |
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| Quelldatensatz | uspto-grants-1985_04 |
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| ORD ID | ord-917d616c80ac4359ad0270951878f8b6 |
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| Quellennotiz | uspto-grants-1985_04 |
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