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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489919Generated: October 25, 2026

Carbon Dioxide → 2-tert-Butyl-6-methoxy-8-nitroquinoline

https://huagongshe.com/reaction/489919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSulfuric AcidHCID 1118—
ReactantPivalic acidHCID 6417—
Reactant6-Methoxy-8-nitroquinolineHCID 6822—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium PersulfateHCID 62648—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-tert-Butyl-6-methoxy-8-nitroquinolineHCID 1128842862%

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Methoxy-8-nitroquinoline (1 mmol) (scheme 1) was dissolved in CH3CN (5 mL) while reaction mixture was warmed to 70° C. Silver nitrate (0.6 mmol), trimethylacetic acid (2.5 mmol), and 10% H2SO4 (10 mL) was then added to the reaction mixture. A freshly prepared solution of ammonium persulfate (3 mmol) in water (10 mL) was added drop wise to the pre-heated (70° C.) mixture during 10 minutes. The heating source was then removed and reaction proceeded with evolution of carbon dioxide. After 10 minutes, reaction mixture was poured onto ice, and resulting mixture was made alkaline with addition of 30% NH4OH. Extracted with ethyl acetate (4×50 mL), and combined extracts were washed with NaCl solution (2×10 mL). Dried over Na2SO4 and solvent removed in vacuo to afford oil, which on flash column chromatography over silica gel (230-400 mesh) gave 2-tert-Butyl-6-methoxy-8-nitroquinoline in good yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979740B2
Source datasetuspto-grants-2005_12
ORD IDord-7ccfa30617374852b115736b0fcf0120
Source noteuspto-grants-2005_12