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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407996Generated: November 1, 2026

Isobutylene → HCID 70496424, compound

https://huagongshe.com/reaction/2407996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
ReactantYtterbium triflateHCID 2733225—
Reactant3-Bromo-5-fluorobenzaldehydeHCID 21986246—
ReactantHCID 62414910HCID 62414910—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70496424HCID 7049642440%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 4-amino-N-cyclobutyl-benzenesulfonamide (2.8 g, 12.4 mmol) and 3-bromo-5-fluoro-benzaldehyde (2.7 g, 13.6 mmol) in acetonitrile (150 mL) were added isobutene (2.7 mL, 37.2 mmoll) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (1.54 g, 2.5 mmol). The resulting mixture was stirred at 80° C. for 18 h in sealed tube. The mixture solution 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, 10-40% ethyl acetate in petroleum ether) to afford 2-(3-bromo-5-fluoro-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-sulfonic acid cyclobutylamide (2.3 g, 40%) as a light yellow solid: MS (ESI) M+1=467.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-a7f6a9013402427d838ce3ada1977a7b
Source noteuspto-grants-2014_08