HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665848Generated: October 31, 2026
Allyl glycidyl ether → Glycidoxypropyltrimethoxysilane
https://huagongshe.com/reaction/1665848
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | Trimethoxysilane | HCID 17215 | — |
| Product | Glycidoxypropyltrimethoxysilane | HCID 17317 | — |
Reaction Steps
In the example, allyl glycidyl ether was reacted with trimethoxysilane to form 3-glycidyloxypropyltrimethoxysilane. The reaction was carried out continuously by feeding the raw materials (allyl glycidyl ether: 9.6 kg/h and trimethoxysilane: 8 kg/h) together with the Pt Karstedt catalyst in the presence of acetic acid (0.05% by weight, based on the total mass of reactants) into a tube reactor. The concentration of the catalyst based on metallic platinum was 2 ppm. The Pt Karstedt catalyst was dissolved in 3-glycidyloxypropyltrimethoxysilane. The reaction temperature was about 160° C. The reaction was carried out using an excess of allyl glycidyl ether (molar ratio of allyl glycidyl ether:trimethoxysilane=1.28:1). The reaction mixture formed was composed of:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039646B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-3214acb9d0264e39b687c145b0455a73 |
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| Source note | uspto-grants-2011_10 |
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