HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854603Generated: October 27, 2026
Toluene → Ethylene 5norbornen-2-yl acetate
https://huagongshe.com/reaction/854603
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Bicyclo(2.2.1)hept-5-en-2-ol, 2-acetate | HCID 95688 | — |
| Catalyst | Bis(1,5-cyclooctadiene)nickel | HCID 6433264 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethylene 5norbornen-2-yl acetate | HCID 69727795 | 1,471% |
Reaction Steps
A glass reactor was loaded inside a glove box with L(iPr2)Ni(η1-CH2Ph)(PMe3) (about 20 μmol; 2.00 g of 8.77 mM solution in toluene), Ni(COD)2 (about 50 μmol; 2.50 g of 17.6 mM solution in toluene), 5-norbornen-2-yl acetate (about 1.79 mmol; 3.00 g of 0.517 M solution in toluene) and toluene (about 18.45 g) such that the total volume of the solution was about 30 mL. The glass reactor was sealed inside the glove box and was attached to a vacuum/nitrogen line manifold. Ethylene was fed continuously into the reactor at about 100 psi and the pressurized reaction mixture was stirred at about 20° C. Ethylene was vented after about 60 minutes and acetone was added to quench the polymerization. The precipitated polymer was collected by filtration and dried under high vacuum overnight. About 2.373 g of ethylene/5-norbornen-2-yl acetate co-polymer was obtained. The activity of the catalyst with respect to ethylene consumption was about 70 kg mol−1 h−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259214B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-a55d8cb5408c472996b3de29b8629728 |
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| Source note | uspto-grants-2007_08 |
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