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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166320Generated: October 26, 2026

p-Chlorophenacyl bromide → 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole

https://huagongshe.com/reaction/1166320

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantSodium BicarbonateHCID 516892—
Reactant4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
SolventIsopropanolHCID 3776—
Product2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazoleHCID 2214896955%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (30 mL), 4-chlorophenacyl bromide (1.05 g, 4.48 mmol) was added. After heating the reaction mixture at 80-85° C. for 18 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography (silica gel, hexane/ethyl acetate, 6/4) to give 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole (545 mg, 55%) as a pale yellow solid: mp 169-171° C. Anal. Calc'd. for C22H16N2SO2Cl2: C, 59.60, H, 3.64, N, 6.32, S, 7.23. Found: C, 59.86, H, 3.80, N, 6.10, S, 7.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613789B2
Source datasetuspto-grants-2003_09
ORD IDord-6104702272784d3e8dd530852c4bb167
Source noteuspto-grants-2003_09