HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 6-Fluoro-7-methoxy-2-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Reactant | 4-Fluoro-3-methoxyaniline | HCID 2774533 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 6-Fluoro-7-methoxy-2-methylquinoline | HCID 86707442 | — |
Reaction Steps
To 4-fluoro-3-methoxyaniline (1.0 g, 7.1 mmol) in refluxing 6N HCl (20 mL) was added dropwise (E)-but-2-enal (0.99 g, 14 mmol) and the reaction was heated to reflux for 2 hours. After cooling, the reaction was neutralized with ammonium hydroxide and extracted with DCM. The combined organic phases were dried over MgSO4, filtered and concentrated under reduced pressure to yield 6-fluoro-7-methoxy-2-methylquinoline as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889704B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-eafa2ae0f97448f9b45b7affc89921aa |
| Source note | uspto-grants-2014_11 |