Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 2-Propenoic acid, 3-phenyl- | HCID 8784 | — |
| Edukt | Diisopropyl fumarate | HCID 5357078 | — |
| Katalysator | tert-BUTYL PEROXYPIVALATE | HCID 61238 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Diisopropyl fumarate cinnamic acid | HCID 118090912 | 123,9% |
Reaktionsschritte
A glass ampule having a volume of 75 mL was charged with 50 g (0.25 mol) of diisopropyl fumarate, 6.5 g (0.044 mol) of cinnamic acid and 0.32 g (0.0018 mol) of tert-butyl peroxypivalate as a polymerization initiator and after repeating purging with nitrogen and release of the pressure, sealed in the pressure-reduced state. This ampule was placed in a constant temperature bath at 50° C. and held for 48 hours, thereby performing radical polymerization. After the completion of polymerization reaction, the polymerization product was taken out of the ampule and dissolved in 400 g of tetrahydrofuran. The resulting polymer solution was added dropwise, for precipitation, to 3 L of methanol, and the precipitate was vacuum-dried at 80° C. for 10 hours to obtain 19 g of a diisopropyl fumarate/cinnamic acid copolymer (yield: 34%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09321870B2 |
|---|
| Quelldatensatz | uspto-grants-2016_04 |
|---|
| ORD ID | ord-57f9cfd210af468c8fb8810ca78aee08 |
|---|
| Quellennotiz | uspto-grants-2016_04 |
|---|