Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Catalyst | Tetrarhodium dodecacarbonyl | HCID 9940312 | — |
| Product | Allylamine | HCID 7853 | — |
| Product | HCID 10236113 | HCID 10236113 | — |
Reaction Steps
A 200 ml. flask equipped with a stirrer, thermometer, dropping funnel, CO inlet tube and reflux condenser having a CO outlet tube, was flushed with carbon monoxide, charged with 1.9 milligrams of tetrarhodium dodecacarbonyl (2.5×10-6 mole), 14 grams of allylamine (0.25 mole) and 60 ml. of xylene, and heated in an oil bath maintained at a temperature of 110° C. Thereafter, 41 grams of triethoxy silane (0.25 mole) was dropwise added to the mixture from the dropping funnel over 30 minutes. The reaction was continued at a temperature of 110° C. for 2 hours under stirring and CO flush. It was revealed by gas chromatography that gamma-aminopropyl triethoxy silane was obtained in a yield of 58% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 4.9% on an allylamine basis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888436 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-78d8e2008711425196d5393550c8313f |
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| Source note | uspto-grants-1989_12 |
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