Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | 2-Ethylhexyl acrylate | HCID 7636 | — |
| Edukt | Calcium hydride | HCID 3033859 | — |
| Edukt | HCID 178506892 | HCID 178506892 | — |
| Edukt | HCID 178506944 | HCID 178506944 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Octane-3-yl acrylate | HCID 15748566 | 95% |
Reaktionsschritte
2.0×10-3 mol of CH3OCH2CH2OLi in solution in THF are introduced under nitrogen atmosphere into a predried round bottom flask. 100 ml of predried THF are added followed, with stirring, dropwise, by 1.0×10-3 mol of (Ph)2CHLi in 0.2-molar solution in THF. The mixture is cooled to a temperature of -78° C. with a mixture of acetone and solid carbon dioxide, followed by the addition, still at -78° C., of 0.048 mol of 2-ethylhexyl acrylate previously stirred for 48 hours over calcium hydride, distilled and then treated over fluorenyllithium until the appearance of a yellow colour and distilled over triethylaluminium immediately before the polymerisation. After 10 minutes the reaction is stopped by addition of 5 ml of acidified methanol and the solvent is then stripped off. An ethylhexyl acrylate polymer is obtained in a 95% yield. Analysis of the polymer by GPC shows the following characteristics:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05677387 |
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| Quelldatensatz | uspto-grants-1997_10 |
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| ORD ID | ord-087dc8716601448c8065def6d0b440b6 |
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| Quellennotiz | uspto-grants-1997_10 |
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