Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043256Generated: November 2, 2026

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

https://huagongshe.com/reaction/1043256

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 numberUS08557847B2
Source datasetuspto-grants-2013_10
ORD IDord-52cbe16de9444e84952c8f54cad32f83
Source noteuspto-grants-2013_10