HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737124Generated: October 25, 2026
7-Oxabicyclo(4.1.0)heptane, 3-ethenyl- → Epoxycyclohexylethyltrimethoxysilane
https://huagongshe.com/reaction/1737124
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-Oxabicyclo(4.1.0)heptane, 3-ethenyl- | HCID 7832 | — |
| Reactant | Trimethoxysilane | HCID 17215 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Product | Epoxycyclohexylethyltrimethoxysilane | HCID 18819 | 90% |
Reaction Steps
The apparatus of Example B was charged with 148.8 g (1.2 mol) of 1-vinyl-3,4-epoxycyclohexane, 1.3 g of a carboxylic acid promoter, and 0.15 ml Of 10% chloroplatinic acid catalyst solution. The flask contents were heated to 89° C. and dropwise addition of 122.8 g (1.0 mol) of trimethoxysilane was begun. The reaction temperature was controlled at 90°-95° C. with an ice bath. Reaction was maintained at that temperature for half an hour after completion of addition, which took 18 minutes. Analysis by gas chromatography showed a yield of 90% of 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane. This example demonstrates a standard preparation of 2-(3,4-epoxycyclohexylethyltrimethoxysilane using commercial chloroplatinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE036330 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-369c5ecb60bc4210a35479607be3e2f9 |
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| Source note | uspto-grants-1999_10 |
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