HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → (4-Bromo-3-bromomethyl-phenoxy)-tert-butyl-dimethyl-silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Bromo-3-methylphenoxy)(tert-butyl)dimethylsilane | HCID 17984598 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4-Bromo-3-bromomethyl-phenoxy)-tert-butyl-dimethyl-silane | HCID 19437125 | 30.1% |
Reaction Steps
To a solution of (4-bromo-3-methylphenoxy)(tert-butyl)dimethylsilane (6.97 g) and N-bromosuccinimide (6.21 g) in ethyl acetate (100 mL) was added 2,2′-azobis(isobutyronitrile) (383 mg), and the mixture was refluxed for 17 hr. The mixture was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.65 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09382188B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-3757b5f31c3541aba121606f57cb3e81 |
| Source note | uspto-grants-2016_07 |