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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032496Generated: October 25, 2026

Iodine → Silane, cyclohexyldimethoxy(2-methylpropyl)-

https://huagongshe.com/reaction/1032496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantChlorocyclohexaneHCID 10952—
ReactantIsobutyltrimethoxysilaneHCID 87622—
ReactantMagnesiumHCID 5462224—
Solventtert-Butyl methyl etherHCID 15413—
ProductSilane, cyclohexyldimethoxy(2-methylpropyl)-HCID 14513104—

Reaction Steps

Under an inert gas, 24.3 g magnesium chips (1.0 mol) were combined with about 10 ml methyl-tert-butylether, an iodine crystal and 3.6 g cyclohexylchloride (0.03 mol). To start the reaction, a solution of 152.0 g isobutyltrimethoxysilane (0.85 mol) and 115.0 g cyclohexylchloride (0.97 mol) in 130 ml methyl-tert-butylether was added dropwise, with stirring, to the first mixture at a rate to maintain a moderate reflux. At the end of this addition, the reaction was allowed to reflux for two more hours. After cooling the reaction mixture, 4.8 g methanol (0.15 mol) was added, stirred for a few minutes and then the precipitate was removed by filtration. The filter cake was washed with several portions of methyl-tert-butylether. The solvent was evaporated from the combined filtrates by water vacuum. The remaining residue consisted of 192.5 g (98.4% of the theoretical yield) isobutylcyclohexyldimethoxysilane which had a purity of 98% according to GC. Isobutyldicyclohexylmethoxysilane was not detected by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04958041
Source datasetuspto-grants-1990_09
ORD IDord-a26ad30f1f404dbca25184fe25d06c96
Source noteuspto-grants-1990_09