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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416025Generated: October 25, 2026

Potassium Carbonate → 5'-Chloro-2'-(2-methyl-2-propenyloxy)acetophenone

https://huagongshe.com/reaction/416025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5'-Chloro-2'-(2-methyl-2-propenyloxy)acetophenoneHCID 5829403897.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 5′-chloro-2′-hydroxyacetophenone (0.86 g, 5.0 mmol), potassium carbonate (1.4 g, 10 mmol) and 3-bromo-2-methylpropene (0.56 mL, 5.5 mmol) in anhydrous N,N-dimethylformamide (20 mL) was stirred at 60° C. for 4 hours. After cooling, the reaction mixture was diluted with water (100 mL), and the whole was extracted with ethyl acetate (100 mL). The organic layer was washed with saturated aqueous ammonium chloride solution (50 mL) and brine (50 mL) and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give the title reference compound (1.1 g) as orange oil (Yield 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088817B2
Source datasetuspto-grants-2012_01
ORD IDord-1609479122814f759c812f9af7a87ca2
Source noteuspto-grants-2012_01