Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | Decane | HCID 15600 | — |
| Reactant | Ethoxytrimethylsilane | HCID 15772 | — |
| Reactant | 7-Methyl-1,6-octadiene | HCID 557579 | — |
| Reactant | Triisobutylaluminum | HCID 16682931 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Titanium | HCID 23963 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | Octene-1 7-methyl-1,6-octadiene | HCID 131718731 | — |
Reaction Steps
A 500 ml polymerizer equipped with an agitating element was charged with 142 ml of decane, 100 ml of octene-1 and 8 ml of 7-methyl-1,6-octadiene. Into this solution elevated in temperature to 50° C. were introduced continuously hydrogen and nitrogen at rates of 1 liter and 50 liters per hour, respectively. The polymerizer was then charged with 0.625 mmol of triisobutylaluminum, 0.21 mmol of trimethylethoxysilane and 0.0125 mmol, in terms of titanium atom, of the solid titanium catalyst component [A] to initiate polymerization. After a thirty-minute polymerization at 50° C., the polymerization was stopped by the addition of small amounts of isobutyl alcohol to the system, and the resulting polymer solution was then poured in large amounts of methanol to separate out a copolymer. The copolymer was recovered and dried at 120° C. under reduced pressure overnight to give 12.4 g of octene-1/7-methyl-1,6-octadiene copolymer. The intrinsic viscosity [η], as measured in decahydronaphthalene at 135° C., of the thus obtained copolymer was 6.4 dl/g, and the content of 7-methyl-1,6-octadiene in the copolymer was 6.6 mol %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354828 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-8e0383bbbd9c4b2a96c22c1b03c389eb |
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| Source note | uspto-grants-1994_10 |
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