HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methyl-2-pyrrolidone → Anthrarufin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 9,10-Anthracenedione, 1,2-dinitro- | HCID 42596 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Product | 1,8-Dihydroxyanthraquinone | HCID 2950 | 7.5% |
| Product | Anthrarufin | HCID 8328 | 92.5% |
Reaction Steps
Dinitroanthraquinone (same composition as in Example 2, 18.0 g; 0.06 mole), N-methylpyrrolidone (100 ml) and sodium formate (12.2 g; 0.18 mole) were stirred at 110° C. for 16 hours while air was sparged into the reaction mass. Product work-up as in Example 1 gave a cake of 1.9 g (92.5% 1,5-dihydroxyanthraquinone, 7.5% 1,8-dihydroxyanthraquinone) and a filtrate product of 12.0 g (4.0% 1-hydroxyanthraquinone, 88% 1,5- and 1,8-dihydroxyanthraquinone, 2.7% intermediate and 5.3% dinitroanthraquinones).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04292248 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-3a77e01e32fd4f7e82853e9b8fd56492 |
| Source note | uspto-grants-1981_09 |