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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273145Generated: October 30, 2026

Trichlorosilane → HCID 123708636, compound

https://huagongshe.com/reaction/2273145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichlorosilaneHCID 24811—
ReactantHCID 86684934HCID 86684934—
SolventHexaneHCID 8058—
ProductHCID 123708636HCID 12370863690%

Reaction Steps

In an argon atmosphere, a dilithium(N,N′-bis(1,1,3,3-tetramethylbutyl)-1,2-vinylenediaminide) solution prepared according to the procedure and reagent quantities described in Reference Example-11 was added to a hexane (150 mL) solution containing 25.00 g (184.6 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: 125° C./85 Pa) to obtain 2-chloro-1,3-bis(1,1,3,3-tetramethylbutyl)-1,3-diaza-2-silacyclopent-4-ene (Si(tOctNCHCHNtOct)(H)Cl) as a pale yellow liquid (yielded amount: 57.22 g, yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120825B2
Source datasetuspto-grants-2015_09
ORD IDord-2a537fe0101545fb8dc08822892e8962
Source noteuspto-grants-2015_09