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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408008Generated: October 30, 2026

Methyl 4-aminobenzoate → HCID 70496690, compound

https://huagongshe.com/reaction/2408008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-aminobenzoateHCID 12082—
ReactantYtterbium triflateHCID 2733225—
Reactant5-Bromo-2-methylbenzaldehydeHCID 10420289—
CatalystIsobutyleneHCID 8255—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70496690HCID 7049669073.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-amino-benzoic acid methyl ester (8.25 g, 50 mmol) and 5-bromo-2-methyl-benzaldehyde (12 g, 60 mmol) in acetonitrile (200 mL) were added isobutene (14 mL, 0.2 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (4.65 g, 7.5 mmol). The resulting mixture was stirred at 85° C. for 16 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-(5-bromo-2-methyl-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid methyl ester (7.1 g, 35%) as a light yellow solid: MS (ESI) M+1=402.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-7da7d44afd7749be988f2babaf8c4d82
Source noteuspto-grants-2014_08