HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Anhydride → 4-(4,8-Dimethyl-3,7-nonadienyl) cyclohex-4-ene-1,2-dioic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | beta Farnesene | HCID 15228937 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(4,8-Dimethyl-3,7-nonadienyl) cyclohex-4-ene-1,2-dioic anhydride | HCID 53709990 | — |
Reaction Steps
The (E)-β-farnesene-containing product of Example 1 (6.0 g) and maleic anhydride (2.0 g) in carbon tetrachloride (20 ml) are reacted together at 25° C. for 2 hours. The mixture is then distilled under reduced pressure to give 4-(4,8-dimethyl-3,7-nonadienyl) cyclohex-4-ene-1,2-dioic anhydride as a yellow oil (3.5, 70%; b.p.176°-182° C./0.25τ; nD20 1.5907; M+ (m/z as % base peak): 302 (2.3): δ(CCl4) 1.70 (m, 9H), 2.08 (m, 8H, 2.20-2.70 (m, 4H), 3.36 (m, 2H), 5.16 (m, 2H), 5.70 (br, t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04546110 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-1b9a602cbda843448d72266ed2e8ed76 |
| Source note | uspto-grants-1985_10 |