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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25796Erstellt: 23. Oktober 2026

Potassium Fluoride → 2,2,4-Trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline

https://huagongshe.com/de/reaction/25796

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium FluorideHCID 522689—
EduktThiophene-3-boronic acidHCID 581760—
EduktTrifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl esterHCID 20760320—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,2,4-Trimethyl-6-thiophen-3-yl-1,2-dihydroquinolineHCID 2256653232,1%

Reaktionsschritte

To a dry 50 mL round bottom flask charged with a mixture of trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester (0.50 g, 1.56 mmol), Pd(OAc)2 (0.035 g, 0.156 mmol), di-tert-butylbiphenylphosphine (DTBBPP) (0.093 g, 0.312 mmol), and KF (0.27 g, 4.67 mmol) suspended in THF (5 mL), was added 3-thiopheneboronic acid (0.30 g, 2.33 mmol). The flask was evacuated and flushed three times with argon and the reaction mixture was allowed to stir at room temperature for 2 days. The reaction mixture was filtered through diatomaceous earth and diluted with EtOAc (50 mL). The mixture was sequentially washed with water (10 mL), NaOH (1.0 M, 10 mL), and brine (10 mL). The organic phase was dried over sodium sulfate (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by chromatography (silica gel, 30% dichloromethane in hexanes) to give 2,2,4-trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline (0.128 g, 32%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858627B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-a5b4cd99bc954d7a8d729932cf755d5b
Quellennotizuspto-grants-2005_02