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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273157Generated: October 30, 2026

tert-Octylamine → HCID 123239943, compound

https://huagongshe.com/reaction/2273157

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-OctylamineHCID 61017—
ReactantHCID 15769382HCID 15769382—
Reactant1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasiloleHCID 71334611—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductHCID 123239943HCID 12323994381%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120825B2
Source datasetuspto-grants-2015_09
ORD IDord-496f0ddc501243c58a879be5c187ea40
Source noteuspto-grants-2015_09