Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Nitro-2-oxindole | HCID 230366 | 70% |
Reaction Steps
The 2-indolinone (6.5 g) was dissolved in 25 mL of concentrated sulfuric acid and the mixture maintained at −10-15° C. while 2.1 mL of fuming nitric acid was added dropwise. After the addition of the nitric acid the reaction mixture was stirred at 0° C. for 0.5 hr and poured into ice-water. The precipitate was collected by filtration,. washed with water and crystallized from 50% of acetic acid. The final crystal was then filtered, washed with water and dried under vacuum to give 6.3 g (70%) of 5-nitro-2-indolinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316635B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-d6b91bfcef464f5682f85039bceb60b0 |
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| Source note | uspto-grants-2001_11 |
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