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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982408Generated: November 1, 2026

4-Chlorophenol → HCID 2444863, compound

https://huagongshe.com/reaction/1982408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-oneHCID 1988398—
SolventWaterHCID 962—
ProductHCID 2444863HCID 244486352.2%

Reaction Steps

28.4 g (0.1 mol) of 2-bromoacetyl-5-bromothiophene are heated under reflux with 19.3 g (0.15 mol) of 4-chlorophenol and 27.6 g (0.2 mol) of potassium carbonate in 200 ml of ketone for 3 hours, while stirring. The mixture is then poured into water, and the ether-ketone is extracted with methylene chloride. The organic phase is washed with dilute sodium hydroxide solution and then with water, and is dried over magnesium sulphate. After the organic phase has been evaporated down, the residue is recrystallized from ethanol. 17.3 g (52% of theory) of 2-bromo-thien-5-yl 4-chlorophenoxymethyl ketone of melting point 128°-130° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596815
Source datasetuspto-grants-1986_06
ORD IDord-3ac0f2151258437cb69d9272fb3f75c4
Source noteuspto-grants-1986_06