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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-4-carbonitrile | HCID 58431137 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carbonitrile | HCID 57920578 | 77.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07645755B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-4c657e4ee2764261ae91a0babb4de416 |
|---|
| Source note | uspto-grants-2010_01 |
|---|