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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036898Generated: November 1, 2026

Isobutylene → HCID 67290535, compound

https://huagongshe.com/reaction/1036898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant4-Fluoro-2-methylanilineHCID 67982—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67290535HCID 6729053540%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-fluoro-2-methyl-phenylamine (8.0 g, 64.0 mmol) and 3-bromobenzaldehyde (7.5 mL, 64.0 mmol) in acetonitrile (150 mL) were added isobutene (18.7 mL, 256.7 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (4.7 g, 7.7 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, 10-50% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-6-fluoro-4,4,8-trimethyl-1,2,3,4-tetrahydro-quinoline (8.8 g, 40.0%) as a light yellow solid: LC/MS m/e obsd. (ESI+) [(M+H)+] 348.0 & 350.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-d4e997285d124da3bd48d09ceaff69f1
Source noteuspto-grants-2013_10