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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980398Generated: October 26, 2026

Ethyl Bromide → 4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrol

https://huagongshe.com/reaction/1980398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Fluoro-4'-hydroxybenzophenoneHCID 117666—
ReactantLithiumHCID 3028194—
ReactantHCID 178506846HCID 178506846—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508926
Source datasetuspto-grants-1985_04
ORD IDord-917d616c80ac4359ad0270951878f8b6
Source noteuspto-grants-1985_04