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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391235Generated: October 31, 2026

Sodium Hydroxide → 5-[(3-Chloro-2-fluorophenyl)methyl]-2,4-dimethoxybenzoic acid

https://huagongshe.com/reaction/391235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 24809621HCID 24809621—
SolventIsopropanolHCID 3776—
Product5-[(3-Chloro-2-fluorophenyl)methyl]-2,4-dimethoxybenzoic acidHCID 2480962081%

Reaction Conditions

Temperature70 °C

Reaction Steps

Methyl 5-(3-chloro-2-fluorobenzyl)-2,4-dimethoxybenzoate was dissolved in isopropanol (20 mL), and 1 mol/L aqueous sodium hydroxide solution (30 mL) was added. The mixture was stirred at 70° C. for 3 h, and completion of the reaction was confirmed by HPLC. After cooling the reaction mixture to room temperature, activated carbon (Sirasagi A) (1.0 g) was added. After stirring, the mixture was filtered using powder cellulose (KC FLOCK). The reaction container and the filter were washed with isopropanol (5 mL)/water (5 mL) solution, and combined with the filtrate. Water (20 mL) and hexane (20 mL) were added to the obtained filtrate and, after stirring, the organic layer was removed. The aqueous layer was washed again with hexane (20 mL). The aqueous layer was ice-cooled, methylisopropylketone (50 mL) was added while adding 2 mol/L hydrochloric acid solution (10 mL) dropwise at 10° C. After the addition, the mixture was stirred at room temperature and the aqueous layer was discarded. The organic layer was washed twice with 10% brine (20 mL). After washing, the solvent was evaporated under reduced pressure to give 5-(3-chloro-2-fluorobenzyl)-2,4-dimethoxybenzoic acid (4.8 g, yield 81%, from methyl 5-bromo-2,4-dimethoxybenzoate obtained in Step 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383819B2
Source datasetuspto-grants-2013_02
ORD IDord-b36a9d1f4fae492287586c91c243cf61
Source noteuspto-grants-2013_02