HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 23471363, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Hydroxyanthraquinone | HCID 11796 | — |
| Product | HCID 23471363 | HCID 23471363 | — |
Reaction Steps
In the same system as described for the 2,6-dihydroxy analog, a solution of 0.01 mole of the silated 2-hydroxy-anthraquinone in tetrahydrofuran is treated slowly with a solution of 0.01 mole of the same lithio anion. The reaction is allowed to proceed for two hours at room temperature. This solution of the enamine is hydrolyzed at room temperature by addition of 20 ml. of 90% formic acid solution. The reaction mixture is filtered, washed with water, dried and recrystallized from toluene giving 2-hydroxy-9,10-anthracene dicarboxaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04258181 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-a708f0a226a242abb0bbb7db995b1bfb |
| Source note | uspto-grants-1981_03 |