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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646474Generated: October 25, 2026

Methyl chloroformate → 4-Methoxycarbonyloxy-3-fluorobenzoic acid

https://huagongshe.com/reaction/1646474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantSodium HydroxideHCID 14798—
Reactant3-Fluoro-4-hydroxybenzoic acidHCID 160456—
SolventWaterHCID 962—
Product4-Methoxycarbonyloxy-3-fluorobenzoic acidHCID 53762941—

Reaction Conditions

Temperature-20 °C

Reaction Steps

4-methoxycarbonyloxy-3-fluorobenzoic acid (VI) was synthesized from 3-fluoro-4-hydroxybenzoic acid (V) by reaction of the latter with methyl chloroformate. NaOH (90 mmol) and 3-fluoro-4-hydroxybenzoic acid (30 mmol) were dissolved in water (80 ml) and cooled to -20° C. Methyl chloroformate (45 mmol) was added dropwise to the mixture. The mixture was then stirred with a magnetic stir bar at 5° C. for four hours and left overnight in the refrigerator. The mixture was then acidified to pH 5 to precipitate 4-methoxycarbonyloxy-3-fluorobenzoic acid. The precipitates were filtered and crystallized from acetonitrile to afford the clean product, 4-methoxycarbonyloxy -3-fluorobenzoic acid (VI), in a 77% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180520
Source datasetuspto-grants-1993_01
ORD IDord-a2d77263d4fb44438e5e1929040d716a
Source noteuspto-grants-1993_01