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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036870Generated: November 1, 2026

Isobutylene → HCID 67292122, compound

https://huagongshe.com/reaction/1036870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67292122HCID 6729212240.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-trifluoromethyl-phenylamine (12.6 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, 20-40% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4-dimethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinoline (12.1 g, 40%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 383.9 & 385.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-f10323b2d6eb426f9450eaa2d0f62cdb
Source noteuspto-grants-2013_10