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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992022Generated: October 30, 2026

Azobisisobutyronitrile → 2-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carbonitrile

https://huagongshe.com/reaction/1992022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carbonitrileHCID 58431137—
SolventCarbon TetrachlorideHCID 5943—
SolventEthyl AcetateHCID 8857—
Product2-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carbonitrileHCID 5792057877.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carbonitrile (0.70 g, 3.1 mmol) (as prepared in the previous step) in CCl4 (10 mL) was added NBS (0.61 g, 3.4 mmol) and AIBN (cat), and the mixture heated at 60° C. for 4 h. The reaction was diluted with EtOAc (30 mL) and washed with NaHCO3 (2×30 mL) and brine (30 mL) and the organic layer was dried over Na2SO4 and then concentrated. The title compound was eluted from a 20-g SPE cartridge (silica) with 30% EtOAc/hexane to give 0.73 g (77%) of a yellow solid: Mass spectrum (CI(CH4), m/z) Calcd. for C10H16BrN3OSi, 302.0/304.0 (M+H), found 302.1/304.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645755B2
Source datasetuspto-grants-2010_01
ORD IDord-4c657e4ee2764261ae91a0babb4de416
Source noteuspto-grants-2010_01