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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781867Generated: October 29, 2026

Triethylamine → Ethyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylate

https://huagongshe.com/reaction/1781867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl isocyanoacetateHCID 533707—
Reactant3,4-Dimethoxy-5-nitrobenzoyl chlorideHCID 21928615—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylateHCID 21459162—

Reaction Steps

A solution of 2.5 g of 3,4-dimethoxy-5-nitrobenzoyl chloride in 10 ml of absolute tetrahydrofuran is treated with 1.1 ml of ethyl isocyanoacetate and subsequently with a solution of 3.0 ml of triethylamine in 10 ml of tetrahydrofuran and stirred at room temperature for 48 hours. After distillation of the solvent, the residue is extracted with ethyl acetate/water. The crude product obtained after evaporation is chromatographed on a 20-fold amount of silica gel with ethyl acetate. After recrystallization from ethyl acetate/hexane there is obtained ethyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylate in the form of yellow crystals of m.p. 109°-110°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-eb6ade9b578e419f95798fbe9a0df127
Source noteuspto-grants-1997_05