HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273143Generated: October 31, 2026
Trichlorosilane → 1,3-Diaza-2-silacyclopent-4-ene, 2-chloro-1,3-bis(1-methylpropyl)-
https://huagongshe.com/reaction/2273143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichlorosilane | HCID 24811 | — |
| Reactant | HCID 86684931 | HCID 86684931 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1,3-Diaza-2-silacyclopent-4-ene, 2-chloro-1,3-bis(1-methylpropyl)- | HCID 123251379 | 42% |
Reaction Steps
In an argon atmosphere, a dilithium(N,N′-di-sec-butyl-1,2-vinylenediaminide) solution prepared according to the procedure and reagent quantities described in Reference Example-8 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 6 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./5×102 Pa) to obtain 2-chloro-1,3-di-sec-butyl-1,3-diaza-2-silacyclopent-4-ene (Si(sBuNCHCHNsBu)(H)Cl) as a pale yellow liquid (yielded amount: 18.10 g, yield: 42%). This product was a mixture of a plurality of isomers differing in the steric configuration from each other.
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-b3b25c3e1105424fbc8ba2638fb3fa48 |
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| Source note | uspto-grants-2015_09 |
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