Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxy cinnamic acid | HCID 13245 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86640905 | HCID 86640905 | — |
| Product | HCID 86640906 | HCID 86640906 | — |
Reaction Steps
The 5-norbornene-2-methanol/ethylene copolymer (18.4 g, 0.121 mol) that was polymerized in (2), 4-methoxy cinnamic acid (Aldrich, 21.5 g, 0.121 mol), EDC [1-(3-dimethylaminopropyl)-3-ethylcarboimide hydrochloride] (Aldrich, 37 g, 0.194 mol), and HOBT (1-hydroxybenzotriazole hydrate) (Aldrich, 24.5 g, 0.182 mol) were put into the 2-neck flask having the volume of 250 ml, and then dissolved in 100 ml of DMF. After the temperature was reduced to 0° C., triethylamine (Aldrich, 75 ml, 0.605 mol) was slowly dropped on the reaction solution. After the temperature was increased to normal temperature and maintained for 3 hours, when the reaction was finished, the reaction solution was dropped on a large amount of methanol to precipitate the polymer, and the polymer was filtered to obtain the 5-norbornene-2-methyl-(4-methoxy cinnamate)/ethylene copolymer to which the 4-methoxy cinnamoyl functional group was introduced (yield: 90.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08329841B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-7ed2a3ca1a5f433f9f60c3afc76329bb |
|---|
| Source note | uspto-grants-2012_12 |
|---|