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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980399Generated: October 25, 2026

Ethyl Bromide → alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcohol

https://huagongshe.com/reaction/1980399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Hydroxy-4'-chlorobenzophenoneHCID 123504—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Productalpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of ethyl magnesium bromide prepared from 3.9 g. of magnesium turnings and 17.4 g. of ethyl bromide in 50 ml. of dry ether a solution of 9.3 g. of 4-chloro-4'-hydroxy-benzophenone in 40 ml. of dry ether is added dropwise, with stirring at -10° C., in nitrogen atmosphere. The reaction mixture is allowed to warm up to room temperature, stirred at this temperature for an additional half an hour, and is then poured onto a solution of ammonium chloride in ice water 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. After filtering the solvent is distilled off in vacuo, the residue is decolored with charcoal in methanol, the solution is filtered, and the solvent is evaporated under reduced pressure. The crude mixture is crystallized from a mixture of benzene and ethyl acetate to yield 5.5 g. of the named compound, melting at 148° to 149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508926
Source datasetuspto-grants-1985_04
ORD IDord-53d61037ce724e43bc1c56f669641de6
Source noteuspto-grants-1985_04