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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051729Generated: October 31, 2026

Allyl bromide → 1-allyl-2-bromo-1H-benzo[d]imidazole

https://huagongshe.com/reaction/1051729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
Reactant2-BromobenzimidazoleHCID 2776281—
SolventEthyl AcetateHCID 8857—
Product1-allyl-2-bromo-1H-benzo[d]imidazoleHCID 11807621052%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-bromo-1H-benzo[d]imidazole (0.400 g, 2.04 mmol), allyl bromide (0.35 mL, 4.08 mmol), 1,4-dioxane (15 mL), and 2 M aqueous sodium hydroxide solution (15 mL, 3.00 mmol) stirred for 2 h at 100° C. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (50 mL). The organic phase was separated and washed with brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified via preparative thin layer chromatography (eluting with 20% ethyl acetate/petroleum ether) to afford 1-allyl-2-bromo-1H-benzo[d]imidazole (0.251 g, 52%) as a yellow oil. MS (ESI, pos. ion) m/z 237, 239 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388161B2
Source datasetuspto-grants-2016_07
ORD IDord-7205731dc75748158df4228c83848a72
Source noteuspto-grants-2016_07