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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1036857Erstellt: 26. Oktober 2026

4-Chloroaniline → 2-(3-Bromophenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1036857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChloroanilineHCID 7812—
EduktIsobutyleneHCID 8255—
Edukt3-BromobenzaldehydeHCID 76583—
EduktYtterbium triflateHCID 2733225—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3-Bromophenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinolineHCID 6729125940%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a stirred solution of 4-chlorophenylamine (10.0 g, 78.4 mmol) and 3-bromobenzaldehyde (9.2 mL, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 0-10% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline (11.0 g, 40.0%) as a light yellow solid: LC/MS m/e obsd. (ESI+) [(M+H)+] 350.0 & 352.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08546427B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-09c2f1c3d63145a3be379713e6a58b08
Quellennotizuspto-grants-2013_10