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 | 97.1% |
Reaction Steps
To 4-fluoro-3-methoxyaniline (4.0 g, 28 mmol) refluxing in 6N HCl (50 mL) was added dropwise (E)-but-2-enal (4.0 g, 57 mmol). The reaction was heated to reflux for 2 hours then cooled and neutralized with NH4OH. The organic phase was extracted with DCM. The combined organic phases dried over MgSO4, filtered and concentrated under reduced pressure to provide 6-fluoro-7-methoxy-2-methylquinoline (5.2 g, 96% yield) as a dark brown paste.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889704B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-81cbd557125b4fc397eb629fe3092263 |
| Source note | uspto-grants-2014_11 |