HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893567Generated: October 31, 2026
Potassium Nitrate → 5-Methyl-6-nitro-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/1893567
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 5-Methyl-1-indanone | HCID 10130031 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Methyl-6-nitro-2,3-dihydro-1H-inden-1-one | HCID 16094764 | 55.3% |
Reaction Steps
This step was performed according to the method described in Journal of Medicinal Chemistry, 2006, 49, 7502-7512. 5-Methylindan-1-one (3.27 g, 22.4 mmol) was dissolved in concentrated sulfuric acid (27 ml), a solution of potassium nitrate (2.28 g, 22.6 mmol) in concentrated sulfuric acid (5 ml) was added dropwise over 10 min under ice-cooling with stirring, and the mixture was stirred at the same temperature for 2 hr. The reaction mixture was added to ice water, and extracted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.37 g, yield 55%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513235B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c57ad474deae41e586d4becffb904685 |
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| Source note | uspto-grants-2013_08 |
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