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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036865Generated: October 31, 2026

Isobutylene → HCID 67291316, compound

https://huagongshe.com/reaction/1036865

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 6729131621.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 2-amino-5-chloro-benzoic acid methyl ester (14.5 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, 10-30% 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 (6.7 g, 21.2%) as a light yellow oil: LC/MS m/e obsd. (ESI+) [(M+H)+] 408.0 & 410.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-d86520e6e89c4fc5acada8a6dcc939c3
Source noteuspto-grants-2013_10