HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436866Generated: October 25, 2026
Acetone → 3-(2'-Ethylcaproyloxy)-propyltriethoxysilane
https://huagongshe.com/reaction/436866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | HCID 178506452 | HCID 178506452 | — |
| Catalyst | Mesityl oxide platinum dichloride | HCID 22159533 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-(2'-Ethylcaproyloxy)-propyltriethoxysilane | HCID 21431668 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028384 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-8e6672dc48534c1fa896ff4e336a4c8d |
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| Source note | uspto-grants-1977_06 |
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