Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391241Generated: October 30, 2026

Hydrochloric Acid → 5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acid

https://huagongshe.com/reaction/391241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acid methyl esterHCID 57572869—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acidHCID 5757284193.4%

Reaction Steps

5-(3-Chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acid methyl ester (100 g) obtained in Example 2, Step III was dissolved in 1-methyl-2-pyrrolidinone (500 ml), and 2.5% V/W aqueous alkali solution prepared from 8N-aqueous sodium hydroxide solution (54.7 ml) and water (192.6 ml) was added dropwise with stirring at room temperature. After the dropwise addition, the mixture was stirred for 3.5 hr, and acidified by dropwise addition of 2N-hydrochloric acid (240 ml) with stirring at room temperature. The precipitated crystals were stirred for 2 hr and collected by filtration. The filtrate was washed with 50% methanol aqueous solution (100 ml) and dried at an outer temperature of 70° C. to give 5-(3-chloro-2-fluorobenzyl)-2-fluoro-4-methoxybenzoic acid (89.4 g, yield 93.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383819B2
Source datasetuspto-grants-2013_02
ORD IDord-642d02038d2e4fdfba34fa531f47154f
Source noteuspto-grants-2013_02