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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767306Generated: October 31, 2026

Potassium Carbonate → 1-(2-(Cyclopropylmethoxy)-6-(4-methoxybenzyloxy)phenyl)ethanone

https://huagongshe.com/reaction/1767306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant1-(2-(Cyclopropylmethoxy)-6-hydroxyphenyl)ethanoneHCID 22258773—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
Product1-(2-(Cyclopropylmethoxy)-6-(4-methoxybenzyloxy)phenyl)ethanoneHCID 992337989.2%

Reaction Steps

To a stirred solution of 1-{2-[(cyclopropylmethyl)oxy]-6-hydroxyphenyl} ethanone (56.3 g, 272 mmol) in acetone (1000 mL) was added potassium carbonate (188 g, 1364 mmol), 4-methoxybenzyl chloride (40.9 mL, 300 mmol) and tetrabutyl-ammonium iodide (20.2 g, 54.6 mmol). The mixture was stirred at reflux overnight. The reaction mixture was allowed to cool to room temperature, filtered on Celite®, and then the filtrate was concentrated under reduced pressure. The residue was diluted with water and extracted with ethyl acetate. The separated organic phase was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. Then the resulting white solid was recrystallized from ethanol, collected by filtration, washed with ethanol, and dried under reduced pressure to give 1-{2-(cyclopropylmethoxy)-6-[(4-methoxybenzyl)oxy] phenyl}ethanone as a white solid (79.2 g, yield; 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232909B2
Source datasetuspto-grants-2007_06
ORD IDord-b5476572a5fd4ed7abe652fd450e80c2
Source noteuspto-grants-2007_06