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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036889Generated: October 26, 2026

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

https://huagongshe.com/reaction/1036889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantIsobutyleneHCID 8255—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(2-Bromophenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinolineHCID 6729036340%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-chlorophenylamine (10.0 g, 78.4 mmol) and 2-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-(2-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-573c408cac024d59a955e7cc9be707a3
Source noteuspto-grants-2013_10