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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408038Generated: November 1, 2026

Ethyl Acetate → HCID 70496412, compound

https://huagongshe.com/reaction/2408038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant4-tert-Butylphenylboronic acidHCID 2734320—
ReactantEthyl 2-(3-bromophenyl)-4,4-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylateHCID 70495883—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 70496412HCID 7049641231.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-(3-bromo-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (1.0 g, 2.6 mmol), 4-tert-butylbenzeneboronic acid (0.50 g, 2.6 mmol), bis(triphenylphosphine)palladium (II) chloride (180 mg, 0.26 mmol) and 2 M sodium carbonate (3.9 mL, 7.8 mmol) in dioxane (5 mL) was heated for 3 h at 120° C. After coiling to room temperature, the mixture was treated with ethyl acetate (50 mL) and washed with water (20 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Purification on flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company) (10% ethyl acetate/hexanes) to afford 2-(4′-tert-butyl-biphenyl-3-yl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.36 g, 31%) as a white solid: MS (ESI) M+1=442.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-1a8dbf357fde4477ba5b009b2038f18a
Source noteuspto-grants-2014_08