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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277158Generated: October 30, 2026

Potassium Carbonate → 3-chloro-4-(cyclopropylmethoxy)Benzoic acid

https://huagongshe.com/reaction/2277158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-chloro-4-hydroxybenzoateHCID 77580—
ReactantBromomethylcyclopropaneHCID 81503—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-chloro-4-(cyclopropylmethoxy)Benzoic acidHCID 61379781—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of methyl 3-chloro-4-hydroxybenzoate (10.0 g) in DMF (100 mL) were added potassium carbonate (14.8 g) and (bromomethyl)cyclopropane (7.80 mL), and the mixture was stirred with heating at 70° C. for 1 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 (50 mL) and methanol (50 mL) was added 2 M aqueous sodium hydroxide solution (54 mL), and the mixture was stirred with heating at 50° C. for 2 hr. 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 ethyl acetate to give the title compound (11.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-03c645d0b6684d4f989816ff82676a1f
Source noteuspto-grants-2015_09