Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-Anthracenecarboxylic acid, 9,10-dihydro-4,5-dimethoxy-9,10-dioxo- | HCID 9972777 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18997000 | HCID 18997000 | — |
Reaction Steps
9,10-Dihydro-4,5-dimethoxy-9,10-dioxoanthracene-2-carboxylic acid (10 g) was suspended in dry DMF (130 ml) and cooled to 0° C. Triethylamine (3.89 g) was then carefully added, followed by a solution of diphenylphosphoryl azide (10.57 g) in dry DMF (20 ml). A yellow precipitate was generated during 12 hours stirring at room temperature. The precipitate was collected by filtration and washed with saturated sodium bicarbonate solution (1×100 ml) and water (5×100 ml). Drying in vacuo over silica gel yielded 9,10-dihydro-4,5-dimethoxy-9,10-dioxoanthracene-2-carbonyl azide as a signal yellow powder. Decomposition point: 139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05480873 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-ec77fbc495d844879e0dbdab7557b94b |
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| Source note | uspto-grants-1996_01 |
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