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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036886Generated: November 3, 2026

Isobutylene → HCID 67289773, compound

https://huagongshe.com/reaction/1036886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant4-AminobenzonitrileHCID 13396—
Reactant2-BromobenzaldehydeHCID 81129—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67289773HCID 6728977340.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-aminobenzonitrile (10.0 g, 84.7 mmol) and 2-bromobenzaldehyde (10 mL, 84.7 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)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (11.6 g, 40.0%) as a light yellow solid: LC/MS m/e obsd. (ESI+) [(M+H)+] 341.0 & 343.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-cd9154b3a83145f990dad37183b7c851
Source noteuspto-grants-2013_10