HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659737Generated: October 30, 2026
Ethyl bromopyruvate → 2-(4-Trifluoromethyl-phenylamino)-thiazole-4-carboxylic acid
https://huagongshe.com/reaction/659737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | N-[4-(Trifluoromethyl)phenyl]thiourea | HCID 2777727 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Trifluoromethyl-phenylamino)-thiazole-4-carboxylic acid | HCID 2760753 | — |
Reaction Steps
3-Bromo-2-oxo-propionic acid ethyl ester (0.59 mL) was added to a suspension of (4-trifluoromethyl-phenyl)-thiourea (1 grams), obtained in step (ii) of example-1, in ethanol (20 mL) and refluxed for about 12 hours. The reaction mixture was cooled and the solid obtained was filtered and dissolved in a minimum amount ethanol. 10% sodium hydroxide solution (10 mL) was added and stirred at about 25-35° C. for about 12 hours. The reaction mixture was then diluted with water and acidified with saturated citric acid solution. The solid that precipitated was filtered washed with water and dried to give the product (0.65 grams).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080668B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-402430ac4e514c549109c5c833301de1 |
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| Source note | uspto-grants-2011_12 |
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