Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | HCID 86738467 | HCID 86738467 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Product | HCID 20532697 | HCID 20532697 | — |
Reaction Steps
27.0 parts of triethoxysilane, 0.05 parts phenothiazine, and 250 ppm hexachloroplatinic acid were charged to a three-neck 100 ml round bottom flask equipped with a magnetic stirrer, thermometer, addition funnel, and water condenser with a nitrogen by-pass. 18.4 parts of allylpentachlorophenyl ether prepared as described above was then added to the dropping funnel. Flask contents were heated to 80° C. at which point the allylpentachlorophenyl ether was added dropwise keeping the exotherm below 100° C. by regulation of the addition rate. After the addition was completed (ca. 15 minutes) the total flask contents were heated at 90° C. for 30 minutes then cooled to room temperature. The flask contents were then evaporated under reduced pressure at 60° C. to yield a liquid which was subsequently vacuum distilled through a six-inch heated vigreux column at 1.0 mm Hg. 13.0 parts of 3-(pentachlorophenoxy)propyltriethoxysilane with a boiling point of 216°-245° C. at 1.0 mm Hg was obtained. The product was identified by gas chromatography, infrared and nuclear magnetic resonance spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04338454 |
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| Source dataset | uspto-grants-1982_07 |
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| ORD ID | ord-50d34815a0f94add89661f8519a07624 |
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| Source note | uspto-grants-1982_07 |
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