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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6450Generated: October 26, 2026

Chlorotrimethylsilane → Cyclopentyloxy cyclopentyl dimethoxysilane

https://huagongshe.com/reaction/6450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantCyclopentanolHCID 7298—
ReactantCyclopentyltrimethoxysilaneHCID 9855701—
CatalystSodium MethoxideHCID 10942334—
ProductCyclopentyloxy cyclopentyl dimethoxysilaneHCID 1979381585.1%

Reaction Steps

In a 50 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 5.0 g (0.0262 mole) of cyclopentyl trimethoxysilane, 22.5 g (0.262 mole) of cyclopentyl alcohol and 18.6 mg (0.34 m mole) of sodium methoxide, which were then reacted with each other at room temperature for 2 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 5.4 g (0.0223 mole) of cyclopentyloxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248803
Source datasetuspto-grants-1993_09
ORD IDord-26d59802162f454b919e6a3c67915737
Source noteuspto-grants-1993_09