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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229533Generated: October 26, 2026

Hydrochloric Acid → (2-(4-Bromo-2-fluoro-benzylcarbamoyl)-5-methoxy-phenoxy]-acetic acid

https://huagongshe.com/reaction/2229533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant[2-(4-Bromo-2-fluoro-benzylcarbamoyl)-5-chloro-phenoxy]-acetic acid ethyl esterHCID 22093478—
SolventEthyl AcetateHCID 8857—
Product(2-(4-Bromo-2-fluoro-benzylcarbamoyl)-5-methoxy-phenoxy]-acetic acidHCID 2209345589%

Reaction Steps

A solution of [2-(4-bromo-2-fluoro-benzylcarbamoyl)-5-chloro-phenoxy]-acetic acid ethyl ester (1.23 g, 2.8 mmol) in ethanol (16 mL, 0.18 M) was cooled to 0° C. and treated with aq NaOH (1.25 M, 7.0 mL, 8.7 mmol). After stirring for 2.5 h, the solution was warmed to room temperature and stirred an additional 24 h. Next, the solution was acidified to pH 1-2 with 2 N HCl, diluted with ethyl acetate and washed with saturated aq NaCl. The organic layer was dried over Na2SO4, filtered and concentrated to give [2-(4-bromo-2-fluoro-benzylcarbamoyl)-5-methoxy-phenoxy]-acetic acid as a white solid (1.03 g, 89%): mp 203-204° C.; Rf 0.10 (10% methanol in dichloromethane); 1H NMR (DMSO-d6, 300 MHz) δ 9.02 (br t, J=5.9 Hz, 1H), 7.84, (d, J=8.2 Hz, 1H), 7.50, (br d, J=8.7 Hz, 1H), 7.48-7.29 (m, 2H), 6.69-6.8 0 (m, 2H), 4.87 (s, 2H), 4.49 (d, J=5.8 Hz, 2H), 3.79 (s, 3H). ESI-LC/MS m/z calcd for C17H15BrFNO5: 411.0; found 412.0 (M+1)−. Anal. calcd for C17H15BrFNO5: C, 49.53; H, 3.67; N, 3.40. Found C, 49.48; H, 3.68; N, 3.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420426B1
Source datasetuspto-grants-2002_07
ORD IDord-2eb08a1c914e4e3e855258a64457ac16
Source noteuspto-grants-2002_07