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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1980399Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1980399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktAmmonium ChlorideHCID 25517—
Edukt4-Hydroxy-4'-chlorobenzophenoneHCID 123504—
EduktMagnesiumHCID 5462224—
EduktHCID 178418443HCID 178418443—
LösungsmittelDiethyl EtherHCID 3283—
Produktalpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04508926
Quelldatensatzuspto-grants-1985_04
ORD IDord-53d61037ce724e43bc1c56f669641de6
Quellennotizuspto-grants-1985_04