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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242095Generated: October 25, 2026

Potassium Phosphate, Tribasic → 4-Phenyl-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2242095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Trifluoromethanesulfonyloxy-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl esterHCID 59205182—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-Phenyl-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl esterHCID 59205205—

Reaction Steps

4-Trifluoromethanesulfonyloxy-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester (208 mg, 0.5 mmol), phenylboronic acid (65 mg, 0.55 mmol), tetrakis(triphenylphosphine)palladium(0) (29 mg) and potassium phosphate (159 mg, 0.75 mmol) were heated together in dioxane (5 mL) to 80° C. overnight. The reaction mixture was then diluted with ethyl acetate and washed with brine twice. The organic layer was dried over sodium sulfate, concentrated, and the residue purified by flash column eluted with 30% ethyl acetate in hexane to yield 4-phenyl-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671065B2
Source datasetuspto-grants-2010_03
ORD IDord-8b1e6087ef724ee2b12c396bee48a5da
Source noteuspto-grants-2010_03