Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | Bicyclo[2.2.1]hept-2-ene, 5-methyl- | HCID 101870 | — |
| Reactant | AlEt2I | HCID 16686130 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Methyl-2-Norbornene 1-Hexene | HCID 86736254 | — |
Reaction Steps
500 ml dry benzene cosolvent, 74 ml 5-methyl-2-norbornene, 12 ml of the 1-hexene solution, and 6 ml of the diethylaluminum iodide solution were charged to a dry, nitrogen-purged quart bottle. 7.5 ml of the MoCl5 solution was charged last, and the bottle was shaken. After 80 minutes the reaction was shortstopped using a mixture of 1.5 ml ethanolamine, 10 ml of antioxidant solution (10 grams of 2,2',2"-tris[3(3,5-di-t-butyl-4-hydroxyphenyl)propionyloxy]ethyl isocyanurate in 100 ml benzene), and 1.5 ml Solution A. The polymer cement was coagulated using excess Solution A in a Waring blender. A solid weighing 66.0 grams was recovered after being filtered and vacuum dried at 60° C. It was found to be a ring-opened 5-methyl-2-norbornene/1-hexene copolymer having a DSV of about 1.90.
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-e24f43d8fd9e421394cb678aefbcf604 |
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| Source note | uspto-grants-1979_01 |
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