HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole → HCID 124007216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole | HCID 71334611 | — |
| Reactant | HCID 178420668 | HCID 178420668 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 124007216 | HCID 124007216 | 48% |
Reaction Steps
In an argon atmosphere, 6.54 g (28.1 mmol) of Si(tBuNCHCHNtBu)(H)Cl was dissolved in 20 mL of hexane and after adding a vinyl magnesium chloride tetrahydrofuran solution (1.61 mol/L, 34.5 mL, 55.5 mmol), the resulting solution was stirred at room temperature for 22 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: 85° C./6.1×102 Pa) to obtain 1,3-di-tert-butyl-2-vinyl-1,3-diaza-2-silacyclopent-4-ene (Si(tBuNCHCHNtBu)(H)CHCH2) as a yellow liquid (yielded amount: 3.01 g, yield: 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120825B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-f2b1ff5996fa44408920f92b1b6eafa6 |
| Source note | uspto-grants-2015_09 |