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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443109Generated: November 4, 2026

Triethylamine → 5-Bromo-2-methylthiazole-4-carbonitrile

https://huagongshe.com/reaction/1443109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant5-Bromo-2-methyl-thiazole-4-carboxylic acid amideHCID 68544050—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-methylthiazole-4-carbonitrileHCID 849383—

Reaction Steps

5-Bromo-2-methyl-thiazole-4-carboxylic acid amide (11.3 g, 51.1 mmol) was dissolved in 150 ml dichloromethane and triethylamine (14.2 ml, 102.2 mmol) was added. Trifluoroaceticanhydride (14.3 ml, 102.2 mmol) was added dropwise at 0° C. and the mixture stirred without cooling for 2 hrs. The reaction mixture was quenched with saturated NaHCO3-solution and extracted with ethyl acetate. The organic extract was washed with brine, dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethyl acetate 90:10->20:80 gradient). The desired compound was obtained as a light yellow solid (6.4 g, 62%), MS: m/e=204.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659401B2
Source datasetuspto-grants-2010_02
ORD IDord-ef1297d2f19143f3b6ff2a6a26a94ed0
Source noteuspto-grants-2010_02