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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024425Generated: November 1, 2026

Ethyl 2-(2-(4-nitrophenyl)-2-oxoethylamino)-2-oxoacetate → Ethyl 5-(4-nitrophenyl)-1,3-oxazole-2-carboxylate

https://huagongshe.com/reaction/1024425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(2-(4-nitrophenyl)-2-oxoethylamino)-2-oxoacetateHCID 66572182—
SolventPhosphorus oxychlorideHCID 24813—
ProductEthyl 5-(4-nitrophenyl)-1,3-oxazole-2-carboxylateHCID 2235046260.6%

Reaction Steps

A solution of Ethyl 2-(2-(4-nitrophenyl)-2-oxoethylamino)-2-oxoacetate (step C product, 8.5 g) in POCl3 (55 ml) was refluxed for 6 hours. The reaction mixture was cooled, quenched with ice and neutralized with sodium carbonate. DCM was added to it and the organic and aqueous layers were separated. Organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to get dark brown residue. The residue was chromatographed on silica gel in 2:8 Ethyl acetate:Pet ether to get pale brown colored solid which was crystallized in chloroform/pet ether to yield 4.82 g (60%) of the title compound. 1HNMR (CDCl3, 300 MHz): δ 8.41 (d, 2H), 7.97 (d, 2H), 7.37 (s, 1H), 4.55 (q, 2H), 1.49 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722901B2
Source datasetuspto-grants-2014_05
ORD IDord-8ebde046958945349795d9e368f9fe89
Source noteuspto-grants-2014_05