Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910168Generated: October 29, 2026

Methyl Salicylate → HCID 67414653, compound

https://huagongshe.com/reaction/910168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl SalicylateHCID 4133—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorobenzyl bromideHCID 68007—
SolventDimethylformamideHCID 6228—
ProductHCID 67414653HCID 6741465377%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl salicylate (1.512 g, 9.93 mmol) in N,N-dimethylformamide (15 ml) were added 3-fluorobenzyl bromide (1.3 ml, 10.6 mmol) and potassium carbonate (1.780 g, 12.88 mmol), and the mixture was stirred at 80° C. for 5 hr. Ethyl acetate was added to the reaction mixture, the mixture was washed with water, and the organic layer was dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to give methyl 2-(3-fluorobenzyloxy)benzoate (1.991 g, 7.65 mmol, yield 77%). This was dissolved in methanol (15 ml), 1N-aqueous sodium hydroxide solution (15 ml) was added at room temperature, and the mixture was stirred at 60° C. for 5 hr. The reaction mixture was concentrated under reduced pressure and neutralized with 1N-aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give a carboxylic acid compound 2-(3-fluorobenzyloxy)benzoic acid (1.790 g, 7.27 mmol, yield 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022072B2
Source datasetuspto-grants-2011_09
ORD IDord-9317a306693643b98aa221c2942e14f8
Source noteuspto-grants-2011_09