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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506243Generated: October 31, 2026

3-Hydroxyanthranilic Acid → Methyl 2-(4-fluorophenyl)benzoxazole-4-carboxylate

https://huagongshe.com/reaction/506243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxyanthranilic AcidHCID 86—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-fluorophenyl)benzoxazole-4-carboxylateHCID 5962602726%
Product2-(4-Fluorophenyl)benzoxazole-4-carboxylic acidHCID 59626030—

Reaction Steps

2-(4-fluorophenyl)benzoxazole-4-carboxylic acid was prepared from 3-hydroxyanthranilic acid and 4-fluorobenzoyl chloride as described in Step A of Example 1. The crude product was dissolved in methylene chloride (20 mL) and the resulting solution treated with oxalyl chloride (1 mL) and DMF (0.05 mL). After stirring at room temperature for 6 h, the reaction was quenched by the addition of methanol (10 mL) and stirred at room temperature for a further 71 h. The reaction was then re-concentrated and the resulting solid purified by column chromatography to afford a 26% yield of methyl 2-(4-fluorophenyl)benzoxazole-4-carboxylate as a white solid: 1H NMR (500 MHz, CDCl3) δ 8.36 (dd, J=14.7, 11.8 Hz, 2H), 8.03 (d, J=14.7 Hz, 1H), 7.78 (d, J=15.2 Hz, 1H), 7.42 (t, J=13.2 Hz, 1H), 7.18 (m, 2H), 4.06 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781430B2
Source datasetuspto-grants-2010_08
ORD IDord-72214cb3875c45c395da1366f10bffc0
Source noteuspto-grants-2010_08