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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376337Generated: October 25, 2026

Water → 1-(8-Bromooctyl)-2,4,5-triphenylimidazole

https://huagongshe.com/reaction/1376337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4,5-TriphenylimidazoleHCID 10232—
ReactantSodium hydrideHCID 24758—
Reactant1,8-DibromooctaneHCID 78310—
SolventDimethylformamideHCID 6228—
Product1-(8-Bromooctyl)-2,4,5-triphenylimidazoleHCID 2291643750%

Reaction Conditions

Temperature45 °C

Reaction Steps

2,4,5-Triphenylimidazole (5 g) was added to a suspension of sodium hydride (1.0 g) (50% dispersion in oil, washed with hexane) in dry dimethylformamide (80 ml ) under nitrogen. The reaction was stirred at 45° C. for 1 h, cooled and added, over 1 h to a solution of 1,8-dibromo-octane (30 g) in dry dimethylformamide (100 ml ) under nitrogen. The reaction was stirred at room temperature for 24 h, water was carefully added and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (500 ml ), washed with water (250ml), 2N aqueous hydrochloric acid (250 ml), saturated sodium chloride solution (250 ml ), dried over anhydrous magnesium sulphate and evaporated to dryness in vacuo. Distillation to remove 1,8-dibromooctane and chromatography on silica gel eluted with dichloromethane gave 1-(8-bromooctyl)-2,4,5-triphenylimidazole (4.1 g, 50%) as an oil; NMR d (CDCl3) 0.9-1.7 (12 H, m, 6×CH2), 3.3 (2H, t, BrCH2), 3.9 (2H, t, N--CH2), 7.1-7.7(15H, m, 3×Ph) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663053
Source datasetuspto-grants-1997_09
ORD IDord-ac6a10ae1230449bac6cd2f423fe43ef
Source noteuspto-grants-1997_09