Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Nitrobenzenesulfonic acid | HCID 7387 | — |
| Reactant | 3-Methyl-4-methoxybenzenamine | HCID 67297 | — |
| Solvent | Glycerol | HCID 753 | — |
| Product | 6-Methoxy-7-methylquinoline | HCID 15534898 | — |
Reaction Steps
To 4-methoxy-3-methylaniline (6.7 g) was added concentrated H2SO4 (12.4 mL), followed by glycerin (21.1 g), m-nitrobenzenesulfonic acid (6.53 g), H3BO3 (3.4 g) and FeSO4.7H2O (3.2 g). The mixture was stirred at 140° C. for 1 h. The reaction was cooled to 25° C., quenched with ice-water and neutralized with 30% KOH. The mixture was extracted with DCM (2×), and the combined extracts dried with Na2SO4 and concentrated in vacuo. The crude product was purified by column chromatography (EtOAc) to give 6-methoxy-7-methylquinoline LCMS-ESI+ (m/z): 174.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376392B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1411b03beff943e8ba287b74857f5534 |
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| Source note | uspto-grants-2016_06 |
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