HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (3-(Bromomethyl)phenyl)trimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Trimethyl(M-tolyl)silane | HCID 10866684 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | (3-(Bromomethyl)phenyl)trimethylsilane | HCID 12583977 | 99.1% |
Reaction Steps
A mixture of m-trimethylsilyltoluene (8.22 g, 50 mmol), NBS (8.90 g, 50 mmol), AIBN (0.05 g) and chlorobenzene (50 ml) was heated by means of a heating bath preheated to 110° C. An exothermic reaction started when the reaction mixture reached 80-90° C. and the orange suspension became a colorless solution within minutes. The mixture was cooled down with the aid of an ice-bath, ice water was added and the resulting mixture was extracted with hexane. The organic phase was washed with water, then brine and dried (MgSO4). Filtration through a silica plug (10 g) followed by evaporation of solvents yielded 12.05 g (99%) of 37 as a colorless liquid. Spectroscopic data were identical to those reported in the literature.43
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548042B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-b9a1c361dc1743b78a88c1f5d3b418a9 |
| Source note | uspto-grants-2003_04 |