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HRID 1712055Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1712055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktPhenylboronic AcidHCID 66827—
Edukt4-Trifluoromethanesulfonyloxy-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl esterHCID 59205182—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-Phenyl-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl esterHCID 59205205—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790895B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-fb6c48bd506b487a86f65f81b6ec7870
Quellennotizuspto-grants-2010_09