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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506660Generated: November 1, 2026

Triethylamine → Ethyl 5-(4-chlorophenyl)oxazole-4-carboxylate

https://huagongshe.com/reaction/1506660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantEthyl isocyanoacetateHCID 533707—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(4-chlorophenyl)oxazole-4-carboxylateHCID 2739479—

Reaction Steps

Triethylamine (20 mL, 144 mmol) was added to a solution of 4-chlorobenzoyl chloride (8.4 g, 48 mmol) in THF (100 mL) at 0° C. Ethyl 2-isocyanoacetate (6.0 g, 53 mmol) was added dropwise and the resulting solution was stirred at room temperature for 1 h. The reaction mixture was partitioned between EtOAc and water. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica column with ethyl acetate and hexanes as eluents to give the desired compound. MS (m/z) 252.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09220710B2
Source datasetuspto-grants-2015_12
ORD IDord-154d0ca150844c3bb7959b249e4d05d0
Source noteuspto-grants-2015_12