HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorodimethylsilane → AC1LBHMA
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Product | AC1LBHMA | HCID 582874 | 177.6% |
Reaction Steps
The Grignard reagent of trimethylchloromethylsilane (TMCMS) was prepared by reaction of 12.3 g (0.1 mol) TMCMS and 2.88 g (0.12 mol) magnesium chips in THF (50 mL). The Grignard reagent was then added dropwise into 9.46 g (0.1 mol) dimethylchlorosilane (DMCS), which dissolved in THF (50 mL). The mixture was stirred at room temperature overnight and quenched with 20 mL HCl-acidified water, and then extracted with diethylether (100 mL). The organic layer washed with distilled water three times and dried with anhydrous sodium sulfate. The mixture was purified by distillation at 118-119° C. to yield 13.0 g (89%) (trimethylsilylmethyl)dimethylsilane product as a clear, colorless fluid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700797B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-8c15e035e2484af0ba5213e175bc4c80 |
| Source note | uspto-grants-2010_04 |