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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636740Generated: October 29, 2026

Imidazole → HCID 18434133, compound

https://huagongshe.com/reaction/1636740

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 numberUS06034275
Source datasetuspto-grants-2000_03
ORD IDord-2e6cd641b4de44c3bd7222794810fd4b
Source noteuspto-grants-2000_03