HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinizarin → 1,4-Bis(octyloxy)anthracene-9,10-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinizarin | HCID 6688 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,4-Bis(octyloxy)anthracene-9,10-dione | HCID 68441317 | 37.7% |
Reaction Steps
1,4-dihydroxyanthracene-9,10-dione (5.0 g, 20.6 mmol), 1-bromooctane (10.0 g, 51.8 mmol), and potassium carbonate (37 g, 0.268 mol) was mixed in N,N-dimethylformamide and heated at 90° C. for 7 h after which the potassium carbonate was filtered off. The reaction mixture was quenched with water and extracted three times with ether. The ether was then washed three times with 1M HCl, one time with water, and evaporated to give a dark yellow solid. This solid was recrystallised in methanol to yield 1,4-bis(octyloxy)anthracene-9,10-dione (1.81 g, 3.88 mmol) as a yellow solid. 1H-NMR (CDCl3, δ): 0.89 (t, 6H), 1.2-1.4 (m, 16H), 1.53 (m, 4H), 1.93 (m, 4H), 4.10 (t, 4H), 7.30 (s, 2H), 7.71 (m, 2H), 8.16 (m, 2H) MS MALDI-TOF (m/z): 464.328
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09343198B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-555a9ae8fe2840619383765dd74b0a95 |
| Source note | uspto-grants-2016_05 |