HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527126Generated: October 26, 2026
Trifluoroacetic acid → 2-Hydroxy-2-(4-isopropyl-2-methoxyphenyl)-4-nitro-2H-inden-1,3-dione
https://huagongshe.com/reaction/527126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1H-Indene-1,3(2H)-dione, 2,2-dihydroxy-4-nitro- | HCID 157712 | — |
| Reactant | 2-Isopropylanisole | HCID 270623 | — |
| Product | 2-Hydroxy-2-(4-isopropyl-2-methoxyphenyl)-4-nitro-2H-inden-1,3-dione | HCID 71476970 | 16% |
Reaction Steps
A solution of 4-nitro-2,3-dihydro-1H-inden-1-one (4.00 g, 20.9 mmol) in 1,4-dioxane (40 ml) and glacial acetic acid (4 ml) was added with selenium dioxide (5.10 g, 46.03 mmol), and refluxed for 3 hrs. After filtration at high temperature, the filtrate was concentrated to afford 2,2-dihydroxy-4-nitro-2H-inden-1,3-dione (4.67 g, 100%). To a solution of 2,2-dihydoxy-4-nitro-2H-inden-1,3-dione (4.67 g, 20.9 mmol) in TFA (10 ml) was added isopropyl anisole (3.14 g, 20.9 mmol), followed by stirring at 60° C. for 6 hrs. The reaction mixture was concentrated in a vacuum, and extracted with aq. sodium bicarbonate and ethylacetate. The concentrated organic layer was purified using column chromatography (ethylacetate:hexane=1:4) to afford the title compound (1.19 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346749B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8e1f3d5d2bff4d91a38439481b17143a |
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| Source note | uspto-grants-2016_05 |
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