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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306480Generated: October 31, 2026

Imidazole → HCID 18434133, compound

https://huagongshe.com/reaction/2306480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18434103HCID 18434103—
SolventDimethylformamideHCID 6228—
ProductHCID 18434133HCID 1843413335.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 68 mg of imidazole in 4 ml of DMF is added dropwise to a suspension of 44 mg of 55% sodium hydride in 4 ml of DMF. After heating the mixture to 70° C. a solution of 441 mg of (E)-[4-(4-bromo-but-2-enyloxy)-phenyl]-(4-bromo-phenyl)-methanone in 12 ml of DMF is added dropwise. Then, the mixture is stirred at 70° C. for a further 1 h. and, after cooling, poured into 5 ml of water and concentrated. The residue is treated with water and extracted with methylene chloride. The organic phases are washed with saturated sodium chloride solution, dried and evaporated. The residue is purified on silica gel with toluene/acetone/triethylamine (70:29:1). The (E)-(4-bromo-phenyl)-[4-(4-imidazol-1-yl-but-2-enyloxy)-phenyl]-methanone (140 mg) is obtained as the beige solid base which is converted into the hydrochloride, MS: m/e 397 (M, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441177B1
Source datasetuspto-grants-2002_08
ORD IDord-cadb77d645e545bbb81a22f345f3d9f6
Source noteuspto-grants-2002_08