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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708660Generated: November 3, 2026

Chlorotrimethylsilane → HCID 18959769, compound

https://huagongshe.com/reaction/1708660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Methyl-2-butanolHCID 6405—
ReactantSodium ethoxideHCID 2723922—
ReactantCyclopentyl(triethoxy)silaneHCID 16217491—
ProductHCID 18959769HCID 1895976979%

Reaction Steps

In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 20.5 g (0.0882 mole) of cyclopentyl triethoxysilane, 128 g (1.46 mole) of tert-amyl alcohol and 0.953 g (14.0 m mole) of sodium ethoxide, which were then reacted with each other in an oil bath of 105° C. for 24 hours under stirring. Subsequently, trimethylchlorosilane was added to neutralize the alkali. Then, 19.0 g (0.0693 mole) of tert-amyloxy cyclopentyl diethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359114
Source datasetuspto-grants-1994_10
ORD IDord-99cf4fef9a6c476d8d820db9503b7b79
Source noteuspto-grants-1994_10