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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504248Generated: October 30, 2026

3,7-Dimethyloctyl trichlorosilane → 3,7-Dimethyloctyl-n-hexyl-dichlorosilane

https://huagongshe.com/reaction/1504248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,7-Dimethyloctyl trichlorosilaneHCID 124015114—
ReactantHCID 178444609HCID 178444609—
SolventTetrahydrofuranHCID 8028—
Product3,7-Dimethyloctyl-n-hexyl-dichlorosilaneHCID 12325791573%

Reaction Steps

Tetrahydrofuran (50 ml) and 3,7-dimethyloctyl trichlorosilane (11.0 g, 40.0 mmol) were placed in a 200 mL four-necked flask in a nitrogen atmosphere, and cooled to −20° C. n-hexyl magnesium bromide (Sigma-Aldrich Co. LLC., 2.0 M, 21 ml) was added dropwise, and the mixture was agitated for 1 hour at 10° C. or less. The temperature was raised gradually to room temperature over the course of about 1 hour, and the mixture was left standing overnight. The precipitated salt was filtered out, the tetrahydrofuran was removed by concentration under reduced pressure, and distillation under reduced pressure was performed to obtain the target 3,7-dimethyloctyl-n-hexyl-dichlorosilane (Compound G18) (127-130° C./0.26 Torr, 9.5 g, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212254B2
Source datasetuspto-grants-2015_12
ORD IDord-90a5aacc3129407d8777abe56f9a0da3
Source noteuspto-grants-2015_12