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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772576Generated: November 2, 2026

HCID 21259639, compound → HCID 123309382, compound

https://huagongshe.com/reaction/1772576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21259639HCID 21259639—
ReactantHCID 178443577HCID 178443577—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 123309382HCID 12330938249%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trichloro(2-ethylhexyl)silane (synthesized in accordance with J. Am. Chem. Soc. 2008, 130, 16144-16145, 24.8 g) was placed in a 300 mL four-necked flask in a nitrogen atmosphere, and dissolved in tetrahydrofuran (100 mL). The resulting solution was cooled to 0° C., and a solution of n-octyl magnesium bromide in diethyl ether (Sigma-Aldrich Co. LLC., 2.00 M, 50.0 mL) was added dropwise. The reaction solution was agitated for about 30 minutes at 7° C., and then agitated for about 3 hours at room temperature. The solvent was then distilled off with an evaporator. Hexane was added to the resulting crude product, which was then filtered, after which the solvent was again distilled off. Finally, distillation purification (111° C., 0.61 torr) was performed to obtain the target dichloro(2-ethylhexyl)n-octylsilane (Compound G6, 15.9 g, yield 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249257B2
Source datasetuspto-grants-2016_02
ORD IDord-2cf1bedd3e04462bbb711e39f6b5ece0
Source noteuspto-grants-2016_02