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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338858Erstellt: 26. Oktober 2026

3-(Trifluoromethyl)aniline → 2-Methyl-7-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/338858

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)anilineHCID 7375—
EduktEthyl AcetateHCID 8857—
EduktCrotonaldehydeHCID 447466—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Produkt2-Methyl-7-(trifluoromethyl)quinolineHCID 2241690428,9%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-f0ad4393e48c40d8b061304cc8e6b1e3
Quellennotizuspto-grants-2014_11