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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
Reactant5-Thiazolecarboxylic acid, 2-amino-4-(trifluoromethyl)-, ethyl esterHCID 67656—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-Bromo-4-trifluoromethyl-thiazole-5-carboxylic acid ethyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602937
Source datasetuspto-grants-1986_07
ORD IDord-33313dbdda094a14988328b1aebbb08e
Source noteuspto-grants-1986_07