Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273144Generated: October 31, 2026

Trichlorosilane → 1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasilole

https://huagongshe.com/reaction/2273144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichlorosilaneHCID 24811—
ReactantHCID 72325861HCID 72325861—
SolventHexaneHCID 8058—
Product1,3-Di-tert-butyl-2-chloro-2,3-dihydro-1H-1,3,2-diazasiloleHCID 7133461183%

Reaction Steps

In an argon atmosphere, a dilithium(N,N′-di-tert-butyl-1,2-vinylenediaminide) solution prepared according to the procedure and reagent quantities described in Reference Example-9 was added to a hexane (50 mL) solution containing 25.20 g (186.0 mmol) of trichlorosilane, and the mixture was stirred at room temperature for 3 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: 80° C./3.8×102 Pa) to obtain 2-chloro-1,3-di-tert-butyl-1,3-diaza-2-silacyclopent-4-ene (Si(tBuNCHCHNtBu)(H)Cl) as a colorless liquid (yielded amount: 35.58 g, yield: 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120825B2
Source datasetuspto-grants-2015_09
ORD IDord-73ccfe17e6f848d889aaa3431f0a3edb
Source noteuspto-grants-2015_09