HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345511Generated: October 25, 2026
Triethoxysilane → (But-2-enyloxypropyl)triethoxysilane
https://huagongshe.com/reaction/345511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | Allyl but-2-enyl ether | HCID 53661857 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | 1-Octene | HCID 8125 | — |
| Solvent | Platinum tetrachloride | HCID 26031 | — |
| Product | (But-2-enyloxypropyl)triethoxysilane | HCID 54048325 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057549 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-c600125b81764147ae5aa53a62b29497 |
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| Source note | uspto-grants-1991_10 |
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