HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichlorosilane → 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | HCID 72325861 | HCID 72325861 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole | HCID 71334611 | 83% |
Reaction Steps
In an argon atmosphere, a dilithium(N,N′-di-tert-butyl-1,2-vinylenediaminide) solution prepared according to the procedure and reagent quantities described in Reference Example-9 was added to a hexane (50 mL) solution containing 25.20 g (186.0 mmol) of trichlorosilane, and the mixture was stirred at room temperature for 3 hours. Insoluble matters produced were separated by filtration, and the solvent was removed by distillation from the filtrate under atmospheric pressure. The obtained residue was distilled under reduced pressure (distillation temperature: 80° C./3.8×102 Pa) to obtain 2-chloro-1,3-di-tert-butyl-1,3-diaza-2-silacyclopent-4-ene (Si(tBuNCHCHNtBu)(H)Cl) as a colorless liquid (yielded amount: 35.58 g, yield: 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120825B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-73ccfe17e6f848d889aaa3431f0a3edb |
| Source note | uspto-grants-2015_09 |