Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butene | HCID 7844 | — |
| Reactant | 2-Norbornene | HCID 10352 | — |
| Reactant | AlEt2I | HCID 16686130 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Norbornene 1-Butene | HCID 86736257 | — |
Reaction Steps
500 ml dry benzene cosolvent, 77 ml 2-norbornene solution, 10 ml of the 1-butene 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. Polymerization occurred so rapidly that the reaction was terminated after 7-8 minutes using a mixture of 1.5 ml ethanolamine, 10 ml of an 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 ml ethanol. The polymer cement was allowed to stand for about 12 hours and coagulated using excess Solution A in a Waring blender. A slightly yellow solid formed and was filtered and vacuum dried at 60° C. The solid weighed 57.4 grams after drying. It was a ring-opened 2-norbornene/1-butene copolymer having a DSV of about 2.3.
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-5761063912194cd2af00e6a1c6c2c493 |
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| Source note | uspto-grants-1979_01 |
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