Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Onychine | HCID 72584 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 3520910 | HCID 3520910 | 67% |
Reaction Steps
A mixture of 35.2 ml of 98.9% strength sulfuric acid with 35.2 ml of 99% strength nitric acid was added dropwise at from +5° to 10° C. to a solution of 15.6 g (0.08 mol) of 4-methyl-5H-indeno[3,2-b]-pyridin-5-one in 35.2 ml of conc. sulfuric acid in the course of 1 hour. After stirring at 25° C. for 14 hours and additionally stirring at 70° C. for 4 hours, the mixture was cooled to 20° C., stirred into 500 g of ice and brought to pH 10 with a 50% strength aqueous sodium hydroxide solution. The mixture was extracted with ethyl acetate, the combined extracts were concentrated under reduced pressure and the residue was crystallized at +10° C. using 30 ml of ether. 13 g (67% of theory) of 4-methyl-7-nitro-5H- indeno[3,2-b]pyridin-5-one were obtained as yellow crystals of m.p. 225°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05637554 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-7f4c48b6e1fa4a6a816c90e1d6dd4030 |
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| Source note | uspto-grants-1997_06 |
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