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HRID 1036868Erstellt: 25. Oktober 2026

Isobutylene → 2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrile

https://huagongshe.com/reaction/1036868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyleneHCID 8255—
Edukt3-BromobenzaldehydeHCID 76583—
EduktYtterbium triflateHCID 2733225—
Edukt4-Amino-3-methylbenzonitrileHCID 7010316—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3-Bromophenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydroquinoline-6-carbonitrileHCID 6728998726,2%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a stirred solution of 4-amino-3-methyl-benzonitrile (10.3 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, 10-30% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4,8-trimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (7.3 g, 26.1%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 355.0 & 357.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08546427B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-1d2e55a5f4514e8b9eb0a1c1afb69f7f
Quellennotizuspto-grants-2013_10