Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | Bicyclo[2.2.1]hept-2-ene, 5-octyl- | HCID 15701270 | — |
| Reactant | AlEt2I | HCID 16686130 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Octyl-2-Norbornene 1-Hexene | HCID 86736261 | — |
Reaction Steps
50 ml dry toluene cosolvent, 7 ml 5-octyl-2-norbornene (containing about 15 wt.% dicyclopentadiene trimer impurity), 8 ml 1-hexene solution, and 0.6 ml diethylaluminum iodide solution were charged to a dry nitrogen-purged 7 oz. bottle. 0.75 ml of the MoCl5 solution was charged last. After about 1 hour the reaction was shortstopped using a mixture of ethanolamine, Solution A and 2 ml of an antioxidant solution (0.1 g/ml of 2,2'-methylenebis[4-methyl-6-t-butylphenol] in toluene). The polymer cement was coagulated using excess Solution A in a Waring blender. The solid recovered after being filtered and vacuum dried at 60° C. was found to be a terpolymer of octylnorbornene, dicyclopentadiene trimer and 1-hexene. Tg was measured and the value adjusted to compensate for the trimer impurity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04136248 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-2fc9189d04f148d58f07631b68fbe9ea |
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| Source note | uspto-grants-1979_01 |
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