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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708658Generated: October 30, 2026

tert-Butanol → HCID 15219058, compound

https://huagongshe.com/reaction/1708658

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium ethoxideHCID 2723922—
ReactantCyclopentyl(triethoxy)silaneHCID 16217491—
ProductHCID 15219058HCID 1521905864.2%

Reaction Steps

In a 500 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 29.3 g (0.129 mole) of cyclopentyl triethoxysilane, 165.9 g (2.24 mole) of tert-butyl alcohol and 2.06 g (30.3 m mole) of sodium ethoxide, which were then reacted with each other in an oil bath of 85° C. for 24 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 21.6 g (0.0828 mole) of tert-butoxy cyclopentyl diethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359114
Source datasetuspto-grants-1994_10
ORD IDord-86c2e2d6d93745adab12d89beb7bc775
Source noteuspto-grants-1994_10