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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
Reactant2-Thiazolamine, 4-(trifluoromethyl)-HCID 1201417—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-4-(trifluoromethyl)-1,3-thiazoleHCID 2314988724%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994196B2
Source datasetuspto-grants-2011_08
ORD IDord-a61a544eec764607878ecb9d6acd7b3d
Source noteuspto-grants-2011_08