Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-6-nitroquinoline | HCID 69172 | — |
Reaction Steps
4-Nitroaniline (6 g, 38 mmol) was dissolved in HCl (6N, 200 mL), the mixture was heated at 100° C. A solution of (E)-but-2-enal (7.2 mL, 76 mmol) in toluene (60 mL) was added dropwise, and the reaction was heated at 100° C. overnight. The reaction mixture was cooled to room temperature and basified with aqueous KOH until pH=12. The mixture was extracted with EtOAc and the organic layer was washed with brine and dried over anhydrous Na2SO4. 2-Methyl-6-nitroquinoline was obtained after purification by column chromatography (hexane:EtOAc=20:1) (5.8 g, 81.2%). MS [M++1]=189, LC-MS: tR=1.64 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119660B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-d919816ad2b74e698f0c1f1085a3b3bd |
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| Source note | uspto-grants-2012_02 |
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