Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | Allylamine | HCID 7853 | — |
| Product | HCID 10236113 | HCID 10236113 | — |
Reaction Steps
A three-neck flask equipped with a reflux condenser, stirring rod and thermometer was charged with 14 grams of allylamine (0.25 mole), 41 grams of triethoxy silane (0.25 mole), 20 ml. of p-xylene and 0.1% by mole (calculated as rhodium), per mole of triethoxysilane, of [Rh(μ-P Ph2) (COD)]2, that is [rhodium(μ-diphenyl phosphide) (1,5-cyclooctadiene) dimer], and heated on an oil bath maintained at a temperature of 110° C. About 1 hour after the beginning of the reaction, the reaction temperature reached 110° C. At the end of the period the reaction mixture was subjected to gas chromatography analysis. It was found that gamma-aminopropyl triethoxy silane was obtained in a yield of 81% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 0.7% on a triethoxy silane basis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04897501 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-e97171a3f19846d1bd33566ebb6b07ca |
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| Source note | uspto-grants-1990_01 |
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