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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341329Generated: October 31, 2026

O-Xylene → HCID 21439246, compound

https://huagongshe.com/reaction/341329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantTriethoxysilaneHCID 13830—
ReactantTrimethoxysilaneHCID 17215—
ReactantCyclohexane, 1,2,4-triethenyl-HCID 96529—
CatalystPlatinumHCID 23939—
ProductHCID 21439246HCID 21439246—
ProductHCID 66694494HCID 66694494—
ProductHCID 69670692HCID 69670692—

Reaction Conditions

Temperature90 °C

Reaction Steps

(2-Triethoxysilylethyl)divinylcyclohexane was prepared from triethoxysilane and 1,2,4-trivinylcyclohexane using the procedure disclosed in Example 1 of U.S. Pat. No. 7,696,269 for trimethoxysilane and 1,2,4-trivinylcyclohexane. A 5 liter, three-neck round bottomed flask fitted with a heating mantle, mechanical stirrer, addition funnel, Friedrich condenser, nitrogen inlet and thermocouple/temperature controller was charged with 1800 g TVCH (11.1 moles) and 3.6 g of a solution (1 wt % Pt) of Karstedt's platinum catalyst in xylene. The contents of the flask were stirred and heated to 90° C. Triethoxysilane (1641 g, 9.99 moles), which had been placed in the addition funnel, was then added slowly over a four hour period to control the exotherm. The temperature remained between 101-109° C. during the addition. The SiH/Vinyl molar ratio in the reaction was 1:3. GC analysis of the crude reaction product gave 21 wt % unreacted TVCH, 48 wt % mono-hydrosilylated product, ((2-Triethoxysilylethyl)divinylcyclohexane), 26.3 wt % bis ((2-Triethoxysilylethyl)vinylcyclohexane and 2.7 wt % tris ((2-Triethoxysilylethyl)cyclohexane. The gravimetric ratio of mono to bis was 1.82.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895770B2
Source datasetuspto-grants-2014_11
ORD IDord-77533884fd6b4a2590e286bc0fe87273
Source noteuspto-grants-2014_11