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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948679Generated: October 31, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 887806, compound

https://huagongshe.com/reaction/1948679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
ProductHCID 887806HCID 88780696.1%

Reaction Steps

24 g of potassium carbonate are added to a solution of 20 g (0.115 mol) of 4-bromophenol and 26.5 g (0.115 mol) of 2-bromo-4′-methoxyacetophenone in 400 of acetonitrile, and the reaction mixture is heated under reflux for five hours. The precipitate is subsequently filtered off, the filtrate is evaporated to dryness, the residue is taken up in 10 ml of water, and the aqueous solution is extracted twice with 10 ml of ethyl acetate each time. The combined organic phases are washed with 10 ml of saturated sodium chloride solution and dried over sodium sulfate. After the solvent has been stripped off, the residue is triturated with 50 ml of diethyl ether, and the resultant crystalline product is filtered off with suction in vacuo, giving 35.5 g of 2-(4-bromophenoxy)-1-(4-methoxyphenyl)ethanone as beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399509B2
Source datasetuspto-grants-2013_03
ORD IDord-0943355fad0e42cf85017c39819d9a0a
Source noteuspto-grants-2013_03