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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419350Erstellt: 25. Oktober 2026

Nitrogen → 2-Ethyl-4-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/419350

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktPotassium CarbonateHCID 11430—
EduktEthylboronic acidHCID 521157—
Edukt2-Bromo-4-fluoro-1-nitrobenzeneHCID 2756993—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-Ethyl-4-fluoro-1-nitrobenzeneHCID 2127736524,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

2-Bromo-4-fluoro-1-nitrobenzene (21.8 g, 100 mmol), ethyl boronic acid (7.5 g, 100 mL), K2CO3 (40 g, 300 mL), dichloro[1,1′-bis(diphenylphosphino)-ferrocene]palladium (II) (6 g) in dioxane (250 mL) and H2O (80 mL) was flushed with N2 and heated at 100° C. overnight. The reaction was diluted with EtOAc and H2O and filtered through Celite®. The organic layer was separated, concentrated and purification by flash chromatography provided the title compound (4.1 g, 24.2 mmol, 24%). 1H NMR (400 MHz, CDCl3) δ ppm 1.30 (t, J=7.78, 3H), 2.92 (q, J=7.78, 2H), 7.01-7.11 (m, 2H), 7.98 (dd, J=8.53 Hz, J=5.53 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093239B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-1bcead23c36d43e8b2a566ac0018f095
Quellennotizuspto-grants-2012_01