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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345511Generated: October 25, 2026

Triethoxysilane → (But-2-enyloxypropyl)triethoxysilane

https://huagongshe.com/reaction/345511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethoxysilaneHCID 13830—
ReactantAllyl but-2-enyl etherHCID 53661857—
CatalystPlatinumHCID 23939—
Solvent1-OcteneHCID 8125—
SolventPlatinum tetrachlorideHCID 26031—
Product(But-2-enyloxypropyl)triethoxysilaneHCID 54048325—

Reaction Conditions

Temperature120 °C

Reaction Steps

About 84 g of allyl but-2-enyl ether are heated under reflux (about 120° C.) in a three-necked flask fitted with a reflux condenser, stirrer and dropping funnel. To this are added dropwise over a period of two hours a solution containing 82 g of triethoxysilane, in which 2 mg of platinum, calculated as the element, are dissolved in the form of a solution of platinum tetrachloride in 1-octene. After heating for an additional five hours under reflux, more than 99 percent of the Si-bonded hydrogen atoms have been converted. The intermediate obtained in this manner, (but-2-enyloxypropyl)triethoxysilane, is purified by distillation at C and at 7 hPa (abs.) and contains 5 percent by weight, based on the total weight of the intermediate, of (but-1-enyloxypropyl)triethoxysilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057549
Source datasetuspto-grants-1991_10
ORD IDord-c600125b81764147ae5aa53a62b29497
Source noteuspto-grants-1991_10