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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1H-Indene-1,3(2H)-dione, 2,2-dihydroxy-4-nitro-HCID 157712—
Reactant2-IsopropylanisoleHCID 270623—
Product2-Hydroxy-2-(4-isopropyl-2-methoxyphenyl)-4-nitro-2H-inden-1,3-dioneHCID 7147697016%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346749B2
Source datasetuspto-grants-2016_05
ORD IDord-8e1f3d5d2bff4d91a38439481b17143a
Source noteuspto-grants-2016_05