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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415037Generated: November 1, 2026

Imidazole → HCID 12151218, compound

https://huagongshe.com/reaction/2415037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantHCID 12151217HCID 12151217—
SolventAcetonitrileHCID 6342—
ProductHCID 12151218HCID 1215121865.2%

Reaction Steps

4-Chloro-5-(1-chlorovinyl)-2-methyl-6-trifluoromethylpyrimidine (1.83 g) was dissolved in acetonitrile (20 ml) under stirring in room temperature. The mixture was added imidazole (1.45 g) and refluxed 3 hr and then cooled to room temperature and added water. The mixture was extracted with chloroform. The chloroform layer was washed with water and brine, respectively and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (chloroform-THF) to give 5-(1-chlorovinyl)-4-imidazol-1-yl-2-methyl-6-trifluoromethyl-pyrimidine (1.34 g) as pale brown oil. 1H-NMR (δ, ppm); 2.82 (s, 3H), 5.78 (d, 1H), 6.03 (d, 1H), 7.21 (br, 1H), 7.87 (br, 1H), 8.55 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818631B1
Source datasetuspto-grants-2004_11
ORD IDord-40defeaa89da4c0d9812cb0c79f3cd46
Source noteuspto-grants-2004_11