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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175720Generated: November 1, 2026

Pyridine → 4-Benzoxazolecarboxylic acid, 2-methyl-, methyl ester

https://huagongshe.com/reaction/2175720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantAnthranilic acid, 3-hydroxy-, methyl esterHCID 205248—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
Product4-Benzoxazolecarboxylic acid, 2-methyl-, methyl esterHCID 1461676279%

Reaction Steps

A solution of methyl 2-amino-3-hydroxybenzoate (167 mg, 1.0 mmol), acetyl chloride (86 mg, 1.1 mmol) and triethylamine (101 mg, 1.1 mmol) in xylene (10 mL) was stirred at 0° C. for 2 h. Pyridine (20 mg, 0.25 mmol) and TsOH (43 mg, 0.25 mmol) were then added and the mixture was heated at reflux overnight. The mixture was then cooled to room temperature, diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with water, brine, then dried over sodium sulfate and the solvent was removed under reduced pressure. The residue was purified by flash chromatography using petroleum ether/ethyl acetate 5:1 (v:v) as eluent to give methyl 2-methylbenzo[d]oxazole-4-carboxylate (151 mg, 79%). LC-MS (ES-API); rt 8.08 min; m/z calculated for C10H9NO3 [M+H]+ 192.1, found 192.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-0ce664a699454f909607dab5067c060a
Source noteuspto-grants-2015_06