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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505639Generated: October 31, 2026

Nitric Acid → 6-methoxy-2,2-dimethyl-7-nitro-2H-1-benzopyran

https://huagongshe.com/reaction/505639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant6-Methoxy-2,2-dimethyl-2H-1-benzopyranHCID 11745424—
SolventAcetic AcidHCID 176—
Product6-methoxy-2,2-dimethyl-7-nitro-2H-1-benzopyranHCID 59134325—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixed solution of acetic acid (6.2 mL) and acetic anhydride (6.2 mL) containing 6-methoxy-2,2-dimethyl-2H-1-benzopyran (3.1 g, 16.4 mmol) was cooled with ice, nitric acid (1.37 mL, 18.0 mmol) was added dropwise and then the mixture was stirred at 0° C. for 1 hour. Upon the completion of the reaction, an aqueous solution of 1 mol/L sodium hydroxide was added to the reaction solution, the resulting solution was extracted with ethyl acetate (150 mL). The organic phase was washed twice with 1 mol/L sodium hydroxide aqueous solution and once with saturated sodium chloride solution. Then, the organic phase was dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by column chromatography (hexane/ethyl acetate=6/1) and the aimed product was obtained as yellow crystal (yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781483B2
Source datasetuspto-grants-2010_08
ORD IDord-146efc3d4a1146a7bf68b1262784ab5d
Source noteuspto-grants-2010_08