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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408080Generated: October 31, 2026

Isobutylene → 7-Quinolinecarboxylic acid, 2-(3-bromophenyl)-1,2,3,4-tetrahydro-4,4-dimethyl-, methyl ester

https://huagongshe.com/reaction/2408080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantBenzoic acid, 3-amino-, methyl esterHCID 78274—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product7-Quinolinecarboxylic acid, 2-(3-bromophenyl)-1,2,3,4-tetrahydro-4,4-dimethyl-, methyl esterHCID 7049745940%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 3-amino-benzoic acid methyl ester (11.3 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, 10-50% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl ester (11.7 g, 40.0%) as a light yellow solid: MS (ESI) M+1=374.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-10d6bf9da24d4c56a3fea62f71462dd9
Source noteuspto-grants-2014_08