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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364653Generated: October 30, 2026

Ethyl Bromide → HCID 20239562, compound

https://huagongshe.com/reaction/364653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant(4-Chlorophenyl){4-[3-(diethylamino)propoxy]phenyl}methanoneHCID 20239560—
SolventDiethyl EtherHCID 3283—
ProductHCID 20239562HCID 20239562—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a Grignard reactant prepared from 7.2 g. of magnesium turnings and 32.6 g. of ethyl bromide in 120 ml. of dry ether a solution of 25.6 g. of 4-chloro-4'-[3-(diethylamino)-propoxy]-benzophenone in 300 ml. of dry ether is added dropwise, with stirring at -30° C. The reaction mixture is refluxed for 30 minutes. After cooling, it is poured onto a solution of ammonium chloride in ice water. The aqueous phase is extracted with ether, the ethereal phase is washed to neutral with water, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure. Distillation of the residue in vacuo yields 15.3 g. of the title compound, boiling at 212° to 214° C./13.3 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04605672
Source datasetuspto-grants-1986_08
ORD IDord-295c275de3ad4009a7b9f416cc8c2ed3
Source noteuspto-grants-1986_08