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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | 6-Methoxy-8-nitroquinoline | HCID 6822 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-tert-Butyl-6-methoxy-8-nitroquinoline | HCID 11288428 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979740B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-7ccfa30617374852b115736b0fcf0120 |
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| Source note | uspto-grants-2005_12 |
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