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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071195Generated: November 1, 2026

Benzopyran → 4H-1-Benzopyran-2-carboxylic acid, 6-nitro-4-oxo-, ethyl ester

https://huagongshe.com/reaction/1071195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzopyranHCID 9211—
ReactantPotassium NitrateHCID 24434—
ReactantEthyl 4-oxo-4H-1-benzopyran-2-carboxylateHCID 26861—
SolventSulfuric AcidHCID 1118—
Product4H-1-Benzopyran-2-carboxylic acid, 6-nitro-4-oxo-, ethyl esterHCID 12163190%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl chromone-2-carboxylate (Example 16) in about 3 mL of sulfuric acid cooled to −10° C. is added about 1 mL potassium nitrate in sulfuric acid. The molar ratio of potassium nitrate to the benzopyran is slightly greater than 1:1. The reaction mixture is stirred at 0° C. for 1 h, the ice bath removed, and the reaction stirred at room temperature until the reaction is complete by HPLC (<3% benzopyran): about 4-6 h. The nitrated benzopyran precipitates as the reaction progresses. The reaction mixture is poured onto ice, and the precipitate is dissolved in ethyl acetate. The ethyl acetate layer is dried, filtered, and evaporated to afford ethyl 6-nitrochromone-2-carboxylate as a light yellow solid (about 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903227B2
Source datasetuspto-grants-2005_06
ORD IDord-7e1f096c064f4d1bab6461c279be65e7
Source noteuspto-grants-2005_06