Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 53826450 | HCID 53826450 | — |
| Product | HCID 44380045 | HCID 44380045 | 44% |
Reaction Steps
Mono-nitro 1,8-diacetylanthraquinone (1 g; M.W. 397; 2.52 mmoles) was added to 10 ml of a mixture tetrahydrofuran: water=20:80 by volume. The mixture was heated to 50° C. under constant stirring followed by addition of NaCN (1.4 g; M.W. 49; 28.57 moles). The reaction mixture was maintained overnight at 50° C. under constant agitation. The resulting mixture was filtered and washed with water. The bright yellow-greenish crystals were dried at 50° C. 3-carboxy-1,8-diacetylanthraquinone was obtained in a 44% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05864048 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-cb836807e47542b4a1d9b6955da4da88 |
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| Source note | uspto-grants-1999_01 |
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