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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408057Generated: November 1, 2026

Isobutylene → HCID 70496808, compound

https://huagongshe.com/reaction/2408057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
ReactantMethyl 4-aminobenzoateHCID 12082—
ReactantYtterbium triflateHCID 2733225—
Reactant5-Bromo-2-ethylbenzaldehydeHCID 54772389—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70496808HCID 7049680866.6%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-amino-benzoic acid methyl ester (1 g, 6 mmol) and 5-bromo-2-ethyl-benzaldehyde (1.2 g, 5.6 mmol) in acetonitrile (40 mL) were added isobutene (1.7 mL, 24 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (0.55 g, 0.9 mmol). The resulting mixture was stirred at 85° C. for 16 h in sealed tube. The mixture was diluted with ethyl acetate (100 mL) and washed with water (50 mL×2) and brine (50 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-(5-bromo-2-ethyl-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid methyl ester (1.5 g, 64%) as a light yellow solid: MS (ESI) M+1=416.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-697d5aed5b704aaf95bf36a4160c25e7
Source noteuspto-grants-2014_08