HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458997Generated: October 29, 2026
Sulfuric Acid → Ethyl 2-bromo-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/458997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-aminothiazole-4-carboxylate | HCID 73216 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-bromo-1,3-thiazole-4-carboxylate | HCID 353965 | 37.5% |
Reaction Steps
A cold solution of sodium nitrite (228 mg, 3.31 mmol) in water (2.0 mL) was added dropwise to a mixture of 2-amino-thiazole-4-carboxylic acid ethyl ester (J. Am. Chem. Soc., 1946, 68, 266) (500 mg, 2.90 mmol), CuSO4 pentahydrate (2.100 g, 8.41 mmol), NaBr (1.134 g, 11.02 mmol), H2SO4 (3.0 mL) and water (3.0 mL) at −5° C. to 0° C. The reaction mixture was stirred at 0° C. for 20 minutes and at room temperature for 1 h. The reaction mixture was adjusted to pH 9 with 1N NaOH (105 mL) and the aqueous solution was washed with CHCl3 (4×50 mL). The organic solutions were combined, dried (MgSO4), filtered and concentrated. Purification by medium pressure chromatography (39:1 hexanes:EtOAc to 19:1 hexanes:EtOAc) provided 2-bromo-thiazole-4-carboxylic acid ethyl ester (257 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192979B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-7a37f23f7f7d4fbe8d8ca6f4ca3af7fc |
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| Source note | uspto-grants-2007_03 |
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