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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708656Generated: October 30, 2026

Chlorotrimethylsilane → HCID 15219057, compound

https://huagongshe.com/reaction/1708656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(+-)-2-ButanolHCID 6568—
ReactantCyclopentyl(triethoxy)silaneHCID 16217491—
CatalystSodium ethoxideHCID 2723922—
ProductHCID 15219057HCID 1521905773.3%

Reaction Steps

In a 500 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 29.6 g (0.127 mole) of cyclopentyl triethoxysilane, 151.1 g (2.04 mole) of sec-butyl alcohol and 286.5 mg (4.21 m mole) of sodium ethoxide, which were then reacted with each other in an oil bath of 50° C. for 10 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 24.2 g (0.0931 mole) of sec-butoxy cyclopentyl diethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 73%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359114
Source datasetuspto-grants-1994_10
ORD IDord-5d569b04d0894c1e997b669ed1413d15
Source noteuspto-grants-1994_10