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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273170Generated: October 29, 2026

N-Methylbutylamine → HCID 86684956, compound

https://huagongshe.com/reaction/2273170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbutylamineHCID 8068—
ReactantHCID 23670121HCID 23670121—
Reactant1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasiloleHCID 71334611—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 86684956HCID 8668495685%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120825B2
Source datasetuspto-grants-2015_09
ORD IDord-15f77a5a7cde4de897056e65e4c36539
Source noteuspto-grants-2015_09