HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650186Generated: November 2, 2026
Ethyl bromopyruvate → Ethyl 2-(3-nitrophenyl)-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/1650186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 3-Nitrobenzene-1-carbothioamide | HCID 12668182 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(3-nitrophenyl)-1,3-thiazole-4-carboxylate | HCID 20060248 | 52.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923886 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-9e70aac967484fdab7e7c7df163a594e |
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| Source note | uspto-grants-1990_05 |
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