HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670748Generated: October 30, 2026
Hydrogen Bromide → 2-Bromo-4-(trifluoromethyl)-1,3-thiazole
https://huagongshe.com/reaction/1670748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Thiazolamine, 4-(trifluoromethyl)- | HCID 1201417 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-(trifluoromethyl)-1,3-thiazole | HCID 23149887 | 24% |
Reaction Steps
2-Amino-4-(trifluoromethyl)thiazole (Wako Pure Chemical Industries, Ltd., 500 mg) was added to 48% aqueous hydrogen bromide (6 ml) and, under ice-cooling, sodium nitrite (266 mg) dissolved in water (1 ml) was added dropwise thereto. The mixture was stirred at 0° C. for 1 hr. A sodium hydrogen sulfite aqueous solution, and then an aqueous sodium hydroxide solution were added, and the mixture was extracted with diethyl ether. The organic layer was dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (elution solvent: ethyl acetate-hexane (1:9)) to give 2-bromo-4-(trifluoromethyl)thiazole (167 mg, yield 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994196B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a61a544eec764607878ecb9d6acd7b3d |
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| Source note | uspto-grants-2011_08 |
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