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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216775Generated: October 30, 2026

Methanol → 3-Fluoro-5-methoxybenzoic acid

https://huagongshe.com/reaction/2216775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant3-Fluoro-5-methoxybenzonitrileHCID 10630684—
Product3-Fluoro-5-methoxybenzoic acidHCID 21942469—

Reaction Steps

In a 50 ml round bottom flask equipped with stir bar and reflux condensor added 3-Fluoro-5-methoxybenzonitrile (0.62 g, 4.10 mmol), methanol (6.2 ml) and sodium hydroxide (6.2 ml, 6N aqueous). Stirred the resulting reaction mixture at 100° C. overnight. Reaction mixture was cooled to room temperature and concentrated in-vacuo. The residue was diluted with dichloromethane (100 ml) and acidified using hydrochloric acid (1N aqueous). The organic phase was separated, sequentially washed with water (100 ml) and brine (100 ml), dried (sodium sulfate) and concentrated in-vacuo, to yield the title compound (0.64 g, 91.%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112595B2
Source datasetuspto-grants-2006_09
ORD IDord-cbb8dfbe018f4a30b06514ff7e711fcc
Source noteuspto-grants-2006_09