HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273170Generated: October 29, 2026
N-Methylbutylamine → HCID 86684956, compound
https://huagongshe.com/reaction/2273170
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylbutylamine | HCID 8068 | — |
| Reactant | HCID 23670121 | HCID 23670121 | — |
| Reactant | 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole | HCID 71334611 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86684956 | HCID 86684956 | 85% |
Reaction Steps
In an argon atmosphere, 5.50 g (23.6 mmol) of Si(tBuNCHCHNtBu)(H)Cl was dissolved in 10 mL of hexane and after adding a lithium butyl(methyl)amide solution (prepared by mixing 14.2 mL of 1.67 mol/L butyllithium hexane solution, 15 mL of tetrahydrofuran and 2.07 g of N-butyl-N-methylamine and stirring the mixture at room temperature for 1 hour), the mixture was stirred at room temperature for 20 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: 109° C./3.3×102 Pa) to obtain 1,3-di-tert-butyl-2-butylmethylamino-1,3-diaza-2-silacyclopent-4-ene (Si(tBuNCHCHNtBu)(H)NBuMe) as a colorless liquid (yielded amount: 5.67 g, yield: 85%).
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-15f77a5a7cde4de897056e65e4c36539 |
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| Source note | uspto-grants-2015_09 |
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