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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732004Generated: October 28, 2026

Sodium Hydroxide → 3-Fluoro-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/732004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDimethyl 5-fluoroisophthalateHCID 4047226—
SolventMethanolHCID 887—
Product3-Fluoro-5-(methoxycarbonyl)benzoic acidHCID 2472892083%

Reaction Steps

A suspension of 5-fluoro-isophthalic acid dimethyl ester (1.7 g, 8.0 mmol) in methanol (41 ml) was treated with 1.0 N sodium hydroxide (7.2 ml, 7.2 mmol). The reaction was left stirring overnight at room temperature. After the solution was concentrated, the residue was dissolved in water and transferred to a separatory funnel. The aqueous layer was washed with dichloromethane (3 times) and then acidified with 1.0 N HCl to pH 2. Ethyl acetate was used to extract the precipitate, which was then washed with brine and dried over anhydrous sodium sulphate. After removal of solvent in vacuo, a total of 1.3 g (83%) of 5-fluoro-isophthalic acid monomethyl ester was isolated as a white solid. 1H NMR (DMSO), δ (ppm): 8.31 (t, 1H), 7.96 (m, 2H), 3.91 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-19b3f5fd1e7c48a484c8e349f1fe1a1a
Source noteuspto-grants-2009_09