HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Trimethyl(M-tolyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 3-Chlorotoluene | HCID 7931 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Trimethyl(M-tolyl)silane | HCID 10866684 | 92% |
Reaction Steps
A solution of m-chlorotoluene (12.66 g, 0.100 mol) and 1,2-dibromoethane (0.5 ml) in THF (20 ml) was added to magnesium turnings (2.67 g, 0.110 mol). The mixture was heated under reflux for 4 h, after which the heating bath was removed and trimethylchlorosilane (11.08 g, 0.102 mol) was added so that gentle reflux was maintained. The mixture was stirred for another 0.5 h and 5% NaHCO3 (100 ml) was then added. The resulting mixture was extracted with CH2Cl2 (3×50 ml), the organic phase was washed with brine and dried (MgSO4). Filtration and evaporation provided 15.05g (92%) of 36 as a pale yellow liquid. Spectroscopic data were identical to those previously reported in the literature.40
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548042B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-bfe9f852ba984c97a54e5a941fac1ebb |
| Source note | uspto-grants-2003_04 |