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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6448Generated: October 26, 2026

Chlorotrimethylsilane → Tert-amyloxy cyclopentyl dimethoxysilane

https://huagongshe.com/reaction/6448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Methyl-2-butanolHCID 6405—
ReactantCyclopentyltrimethoxysilaneHCID 9855701—
CatalystSodium MethoxideHCID 10942334—
ProductTert-amyloxy cyclopentyl dimethoxysilaneHCID 1098860282%

Reaction Steps

In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 10.1 g (0.0531 mole) of cyclopentyl trimethoxysilane, 30.6 g (0.347 mole) of tert-amyl alcohol and 86.4 mg (1.6 m mole) of sodium methoxide, which were then reacted with each other in an oil bath of 105° C. for 4 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 10.7 g (0.0434 mole) of tert-amyloxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248803
Source datasetuspto-grants-1993_09
ORD IDord-44523718c32f4f8db78be90afe1a804e
Source noteuspto-grants-1993_09