HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hexene → 5-Ethyl-2-Norbornene 1-Hexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | Bicyclo(2.2.1)hept-2-ene, 5-ethyl- | HCID 85837 | — |
| Reactant | AlEt2I | HCID 16686130 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Ethyl-2-Norbornene 1-Hexene | HCID 86736258 | — |
Reaction Steps
50 ml dry toluene cosolvent, 7 ml 5-ethyl-2-norbornene, 0.8 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, and the bottle was shaken. After 1 hour the reaction was shortstopped using a mixture of 0.8 ml ethanolamine, 3 ml Solution A and 25 ml toluene. 2 ml of an antioxidant solution was added (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. A solid weighing 5.9 grams was recovered after being filtered and vacuum dried at 60° C. It was found to be a ring-opened 5-ethyl-2-norbornene/1-hexene copolymer with a DSV of about 1.53.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04136248 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-ef4e22ac525f45cebddab40b6d5fc24d |
| Source note | uspto-grants-1979_01 |