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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367747Generated: October 31, 2026

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

https://huagongshe.com/reaction/2367747

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 numberUS08697716B2
Source datasetuspto-grants-2014_04
ORD IDord-8212fc9f67004142a803e6b97b8264a2
Source noteuspto-grants-2014_04