HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746138Generated: October 30, 2026
Hydrogen Bromide → 2-Bromo-4-trifluoromethyl-thiazole-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/746138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | 5-Thiazolecarboxylic acid, 2-amino-4-(trifluoromethyl)-, ethyl ester | HCID 67656 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-trifluoromethyl-thiazole-5-carboxylic acid ethyl ester | HCID 13282759 | — |
Reaction Steps
To a solution of 4.5 g (0.0187 mole) of ethyl 2-amino-4-trifluoromethyl-5-thiazolecarboxylate in 50 ml. of 85% phosphoric acid at -10° C. was added 25 ml. of nitric acid. To this mixture was added dropwise at -10° C. to -5° C. a solution of 4.0 g (0.0579 mole) of sodium nitrite in 20 ml. of water in 30 minutes. This mixture was stirred for 10 minutes at -10° C. to -5° C. and poured into a solution of 2.70 g (0.0187 mole) of freshly prepared cuprous bromide in 20 ml. of hydrobromic acid. A vigorous evolution of gas occurred. The reaction mixture was stirred for 5 minutes and diluted with water. The solid suspension was filtered and air-dried to give 4.8 g of solid which was chromatographed on silica gel using ether/petroleum ether (1:4) as eluant. The first 1 liter of eluate gave 3.7 g of solid which was recrystallized from petroleum ether to give 2.9 g (51%) of the desired product as white needles, m.p. 75.5°-76.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04602937 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-33313dbdda094a14988328b1aebbb08e |
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| Source note | uspto-grants-1986_07 |
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