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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1909148Erstellt: 25. Oktober 2026

Diisopropylamine → Ethyl 5-(2-fluoro-4-methylphenyl)nicotinate

https://huagongshe.com/reaction/1909148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktEthyl 5-bromopyridine-3-carboxylateHCID 140785—
EduktSodium BicarbonateHCID 516892—
Edukt(2-Fluoro-4-methylphenyl)boronic acidHCID 2783132—
EduktTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 5-(2-fluoro-4-methylphenyl)nicotinateHCID 67338384102,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of ethyl 5-bromonicotinate (0.58 g, 2.53 mmol) in acetonitrile (15 mL) and water (5 mL) were added (2-fluoro-4-methylphenyl)boronic acid (0.47 g, 3.04 mmol), 3,3′,3″-phosphinidynetris(benzenesulfonic acid) trisodium salt (0.22 g, 0.38 mmol), palladium(II)acetate (28.4 mg, 0.13 mmol) and diisopropylamine (0.90 mL, 6.32 mmol). The mixture was heated to 80° C. After 1 h, the mixture was cooled to ambient temperature and saturated aqueous NaHCO3 was added. The mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→70% hexanes/ethyl acetate) gave the title compound (0.67 g). MS 260.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08598209B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-394117abaf164211983341ba147be7a0
Quellennotizuspto-grants-2013_12