HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Maleic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 1,7-Octadiene | HCID 19460 | — |
| Product | Maleic Anhydride | HCID 7923 | — |
| Product | 1,9-Decadiene | HCID 15439 | — |
Reaction Steps
This Example shows use alternative dienes to 1,7-octadiene. 1,9-decadiene (55.2 g, 0.40 mol) and maleic anhydride (19.6 g, 0.20 mol) in acetone (200 g) was polymerized in the same apparatus and under the same conditions as Example 4. The yield of desired copolymer was 33.2 g. The 1H NMR showed 17 mole % vinyl octyl protons, 15 mole % saturated octyl protons, and 4.3 mole % phenyl protons from the benzoyl peroxide initiator. Further characterization is presented in Table 2 and in FIG. 2, as discussed below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579403B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-b2a3d8cf703e444093a5edc2b227255f |
| Source note | uspto-grants-2009_08 |