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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408106Generated: November 1, 2026

Isobutylene → HCID 67291951, compound

https://huagongshe.com/reaction/2408106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
ReactantMethyl AnthranilateHCID 8635—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67291951HCID 6729195140%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 2-amino-benzoic acid methyl ester (10 g, 60.5 mmol) and 3-bromobenzaldehyde (8 mL, 60.5 mmol) in acetonitrile (200 mL) were added isobutene (17 mL, 242 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (4.5 g, 7.3 mmol). The resulting mixture was stirred at 90° 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-(3-bromo-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester (9 g, 40%) as a light yellow solid: MS (ESI) M+1=374.0 & 375.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-abab7de40e344387be25703c75fd1b97
Source noteuspto-grants-2014_08