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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267457Generated: November 1, 2026

Sulfuric Acid → Ethyl 2-bromo-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1267457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
ReactantSodium BromideHCID 253881—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductEthyl 2-bromo-1,3-thiazole-4-carboxylateHCID 35396537.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552067B2
Source datasetuspto-grants-2003_04
ORD IDord-9ea932637ed14ffbad8d1120c021b98c
Source noteuspto-grants-2003_04