Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436866Generated: October 25, 2026

Acetone → 3-(2'-Ethylcaproyloxy)-propyltriethoxysilane

https://huagongshe.com/reaction/436866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAllyl AlcoholHCID 7858—
ReactantTriethoxysilaneHCID 13830—
ReactantHCID 178506452HCID 178506452—
CatalystMesityl oxide platinum dichlorideHCID 22159533—
SolventBenzeneHCID 241—
Product3-(2'-Ethylcaproyloxy)-propyltriethoxysilaneHCID 21431668—

Reaction Conditions

Temperature75 °C

Reaction Steps

184 g of 2-ethylcapronic acid allyl ester (prepared from the free acid and allyl alcohol by azeotropic esterification in benzene in the presence of p-toluenesulfonic acid; BP18 : 95° C.; nD20 : 1.4298) was heated to 75° C. in a 3-necked flask provided with stirrer, reflux condenser, internal thermometer and dropping funnel. Then 0.1 ml of an 0.01 molar solution of mesityl oxide-platinum dichloride catalyst complex in acetone was stirred in, and a quantity of 164 g of triethoxysilane was fed in from the dropping funnel within a 6-minute period, during which the temperature rose to 99° C. 10 minutes after the triethoxysilane feed was completed, no more silane hydrogen was analytically detectable. Vacuum distillation of the product yielded 322 g of 3-(2'-ethylcaproyloxy)-propyltriethoxysilane, BP1 : 134°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028384
Source datasetuspto-grants-1977_06
ORD IDord-8e6672dc48534c1fa896ff4e336a4c8d
Source noteuspto-grants-1977_06