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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235293Generated: October 25, 2026

Potassium Nitrate → 4,6-dimethyl-5-nitro-2,3-dihydro-1H-indole-2,3-dione

https://huagongshe.com/reaction/235293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant4,6-dimethyl-1H-indole-2,3-dioneHCID 2386161—
SolventSulfuric AcidHCID 1118—
Product4,6-dimethyl-5-nitro-2,3-dihydro-1H-indole-2,3-dioneHCID 2335443577.2%

Reaction Steps

The method of Cheesman, G. W. H.; J. Chem. Soc. 1170 (1962), was adapted. 4,6-Dimethylisatin (89 mg, 0.50 mmol) was dissolved in concentrated H2SO4 (1.0 mL) at 0° C. for 30 min with stirring, then KNO3 (55 mg, 0.55 mmol, Baker) was added to this solution. The mixture was stirred at 25° C. for 24 h. It was then poured into ice water (5 g). The resulting precipitate was collected by filtration. The precipitate was dissolved in 1N KOH (5 mL) and the small amount of solid was removed by filtration, then the filtrate was acidified to pH 2 with 4N HCl (~1 mL) to give a yellow precipitate. The solid was collected by filtration and was washed with water (2×1 mL), then it was dried in the air at 50° C. for 4 h affording pure (by NMR) title compound (85 mg, 77%) as a yellow powder. Crystallization from acetone/water gave crystals. Mp 278°-80° C. (dec.). IR (KBr, cm-1): 3452, 3225, 2931, 1780, 1742, 1635, 1608, 1535. 1H NMR (DMSO-d6): δ 11.357 (s, 1H), 6.771 (s, 1H), 2.389 (s, 3H), 2.305 (s, 3H). Purity >97.5% by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597922
Source datasetuspto-grants-1997_01
ORD IDord-a01efeeec5694493b00ed9c8dc9b8df2
Source noteuspto-grants-1997_01