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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8367Generated: October 25, 2026

1-Bromo-3-chloropropane → 2'-Methyl-4'-chloropropoxyacetophenone

https://huagongshe.com/reaction/8367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-2-methylacetophenoneHCID 70133—
SolventAcetoneHCID 180—
Product2'-Methyl-4'-chloropropoxyacetophenoneHCID 69377079—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4′-hydroxy-2′-methyl-acetophenone (10.5 g) and 1-bromo-3-chloropropane (7.6 mL) in acetone (70 mL) was treated with potassium carbonate (14.5 g). The mixture was stirred at 50° C. for approximately 18 hours. The reaction mixture was cooled to ambient temperature and partitioned between dichloromethane (200 mL) and water (200 mL). The aqueous layer was washed twice with fresh portions of dichloromethane (200 mL) and brine was used to break any emulsions. The organic fractions were combined, dried over sodium sulfate, and evaporated. The residue was re-dissolved in dichloromethane (100 mL) and washed with 0.5 M sodium hydroxide (100 mL) and brine (100 mL), dried over magnesium sulfate, filtered and evaporated to give the title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087757B2
Source datasetuspto-grants-2006_08
ORD IDord-d09efd5bbd8744ae90df923aa5ef3ad5
Source noteuspto-grants-2006_08