Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | HCID 86684934 | HCID 86684934 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 123708636 | HCID 123708636 | 90% |
Reaction Steps
In an argon atmosphere, a dilithium(N,N′-bis(1,1,3,3-tetramethylbutyl)-1,2-vinylenediaminide) solution prepared according to the procedure and reagent quantities described in Reference Example-11 was added to a hexane (150 mL) solution containing 25.00 g (184.6 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: 125° C./85 Pa) to obtain 2-chloro-1,3-bis(1,1,3,3-tetramethylbutyl)-1,3-diaza-2-silacyclopent-4-ene (Si(tOctNCHCHNtOct)(H)Cl) as a pale yellow liquid (yielded amount: 57.22 g, yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120825B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-2a537fe0101545fb8dc08822892e8962 |
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| Source note | uspto-grants-2015_09 |
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