Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | 3-CHLORO-4-NITRO-1H-INDOLE | HCID 12049863 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 4-Nitro-1,3-dihydro-2H-indol-2-one | HCID 21677874 | — |
Reaction Steps
Phosphoric acid (35 mL of 86%) is added to a solution of 3-chloro-4-nitroindole (1.27 g, 6.46 mmol) in 2-methoxyethanol (50 mL) at 100° C. The resulting brown colored solution is stirred at 95° C. for 3.5 hours. The reaction is cooled to room temperature and then poured into 500 mL of water. The aqueous layer is extracted three times with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate, filtered and the solvents removed by rotary evaporation. The crude material is purified via silica gel column chromatography using 2% methanol/methylene chloride as the eluent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.90 g of slightly impure 4-nitrooxindole as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162818 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-1164e58fe4b44a03800002ee524da014 |
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| Source note | uspto-grants-2000_12 |
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