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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157372Generated: October 25, 2026

Triethylamine → 4-(5-Oxazolyl)-benzamide

https://huagongshe.com/reaction/1157372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium HydroxideHCID 14923—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-(1,3-Oxazol-5-yl)benzoic AcidHCID 2776414—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Oxazolyl)-benzamideHCID 2193099948.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(5-oxazolyl)benzoic acid (1.0 g, 5.46 mmol) and Et3N (552 mg, 5.46 mmol) in 25 mL of THF was cooled to 0° C. and ClCOOi-Bu (745 mg, 5.46 mmol) was added dropwise. After the addition was over, the reaction mixture was stirred for additional 5 min and then aq NH4OH (0.63 mL of 28% solution, 10.46 mmol) was added. After overnight stirring, the solvent was evaporated, the residue was taken up in water and basified to pH 9. The precipitated solid was filtered, washed with water and dried over P2O5 in a vacuum desiccator to provide 500 mg (48%) of the 4-(5-oxazolyl)-benzamide: 1H NMR (DMSO-d6) δ 8.50 (s, 1H), 8.20-7.80 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807683B2
Source datasetuspto-grants-2010_10
ORD IDord-355538ebcbfc4c4f93f143cecff44ea9
Source noteuspto-grants-2010_10