Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | cis,cis-1,5-Cyclooctadiene | HCID 8135 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | 19584-30-6 | HCID 9940312 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| 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 and charged with 1.9 milligrams of tetrarhodium dodecacarbonyl (2.5×10-6 mole), 0.027 gram of 1,5-cyclooctadiene (2.5×10-4 mole) and 60 ml. of xylene. While passing carbon monooxide through the flask at a rate of 10 ml./min., the mixture was heated to a temperature of 120° C. under stirring. To the mixture a mixture of 41 grams of triethoxy silane (0.25 mole) and 14 grams of allylamine (0.25 mole) was dropwise added over a period of 30 minutes. After the addition of the reactants, the reaction was carried out at a temperature of 120° C. for 2.5 hours under CO flush and stirring. It was revealed by gas chromatography that gamma-aminopropyl triethoxy silane was obtained in a yield of 75% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 7.5% 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-5f93aed616cd4f35ab8e5b0357e71d59 |
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| Source note | uspto-grants-1989_12 |
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