Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Octylamine | HCID 61017 | — |
| Reactant | HCID 15769382 | HCID 15769382 | — |
| Reactant | 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole | HCID 71334611 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 123239943 | HCID 123239943 | 81% |
Reaction Steps
In an argon atmosphere, a solution obtained by dissolving 5.14 g (22.1 mmol) of Si(tBuNCHCHNtBu)(H)Cl in 10 mL of hexane was added to a lithium(1,1,3,3-tetramethylbutylamide) solution prepared by adding 10 mL of hexane and 2.94 g (22.8 mmol) of 1,1,3,3-tetramethylbutylamine to 13.8 mL (22.8 mmol) of a hexane solution (concentration: 1.65 mol/L) of butyllithium and stirring the mixture at room temperature for 14 hours, and the resulting mixture was stirred at room temperature for 24 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 sublimated (heating temperature: 180° C./64 Pa) to obtain 1,3-di-tert-butyl-2-(1,1,3,3-tetramethylbutyl)amino-1,3-diaza-2-silacyclopent-4-ene (Si(tBuNCHCHNtBu)(H)NHtOct) as a white solid (yielded amount: 5.85 g, yield: 81%).
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-496f0ddc501243c58a879be5c187ea40 |
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| Source note | uspto-grants-2015_09 |
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