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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktAmmonium ChlorideHCID 25517—
Edukt4-Fluoro-4'-hydroxybenzophenoneHCID 117666—
EduktLithiumHCID 3028194—
EduktHCID 178506846HCID 178506846—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04508926
Quelldatensatzuspto-grants-1985_04
ORD IDord-917d616c80ac4359ad0270951878f8b6
Quellennotizuspto-grants-1985_04