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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277154Generated: October 30, 2026

Potassium Carbonate → 3-(cyclopropylMethoxy)benzoic acid

https://huagongshe.com/reaction/2277154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
ReactantBromomethylcyclopropaneHCID 81503—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(cyclopropylMethoxy)benzoic acidHCID 25019431—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of ethyl 3-hydroxybenzoate (15.0 g) in DMF (150 mL) were added potassium carbonate (25.0 g) and (bromomethyl)cyclopropane (13.1 mL), and the mixture was stirred with heating at 70° C. for 3 hr. The reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate, and washed with saturated brine. The obtained organic layer was subjected to silica gel column chromatography (NH, ethyl acetate), and the solvent was evaporated. To a solution of the obtained residue in a mixed solvent of THF (100 mL) and methanol (50 mL) was added 2 M aqueous sodium hydroxide solution (47 mL), and the mixture was stirred with heating at 60° C. for 40 min. The reaction mixture was allowed to cool to room temperature, and neutralized with 6 M hydrochloric acid, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained solid was washed with diethyl ether/hexane to give the title compound (13.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-5b8660974edc492c893aa49be2b800dc
Source noteuspto-grants-2015_09