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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408096Generated: November 1, 2026

Isobutylene → HCID 67291316, compound

https://huagongshe.com/reaction/2408096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 2-amino-5-chlorobenzoateHCID 78878—
ReactantYtterbium triflateHCID 2733225—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 67291316HCID 6729131645%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 2-amino-5-chloro-benzoic acid methyl ester (9.25 g, 50 mmol) and 3-bromobenzaldehyde (6.4 mL, 55 mmol) in acetonitrile (200 mL) were added isobutene (14 mL, 200 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-(3-bromo-phenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester (8.9 g, 45%) as a light yellow solid: MS (ESI) M+1=408.0 & 410.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-527c56b35d374f1fb0cf52a7951aff9a
Source noteuspto-grants-2014_08