HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-(Trifluoromethyl)aniline → 2-Methyl-7-(trifluoromethyl)quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Crotonaldehyde | HCID 447466 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Methyl-7-(trifluoromethyl)quinoline | HCID 22416904 | 28,9% |
Reaktionsschritte
To a solution of 3-(trifluoromethyl)aniline (12.43 mL, 99.92 mmol) in 6 N HCl (50 mL) in water was added (E)-but-2-enal (18.77 mL, 229.8 mmol) dropwise at reflux. The reaction was stirred at reflux for 3 hours. After cooling to ambient temperature, ethyl acetate (200 mL) was added. The aqueous layer was separated, basified with ammonium hydroxide to about pH 9, and extracted with DCM (2×200 mL). The combined organic layers were dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexane/ethyl acetate) to give 2-methyl-7-(trifluoromethyl)quinoline (6.1 g, 28.9%) as a solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08889704B2 |
| Quelldatensatz | uspto-grants-2014_11 |
| ORD ID | ord-f0ad4393e48c40d8b061304cc8e6b1e3 |
| Quellennotiz | uspto-grants-2014_11 |