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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085496Generated: November 1, 2026

Ethyl bromopyruvate → Ethyl 2-(3-nitrophenyl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1085496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant3-Nitrobenzene-1-carbothioamideHCID 12668182—
SolventEthanolHCID 702—
ProductEthyl 2-(3-nitrophenyl)-1,3-thiazole-4-carboxylateHCID 2006024852.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of ethyl bromopyruvate (2.14 g) in ethanol (5 ml) was added to a suspension of 3-nitrobenzenecarbothioamide (2.00 g) in ethanol (15 ml) at room temperature. The reaction mixture was stirred at 50° C. for 2 hours and ten minutes. The solvent was removed by evaporation under reduced pressure. To the residue was added a saturated aqueous solution of sodium bicarbonate (50 ml) and ethyl acetate (100 ml). The precipitates were collected by filtration and recrystallized from a mixture of chloroform and n-hexane to give ethyl 2-(3-nitrophenyl)-4-thiazolecarboxylate (1.59 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010093
Source datasetuspto-grants-1991_04
ORD IDord-7824e0311eb54006a79b4e1c61ab71f7
Source noteuspto-grants-1991_04