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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1776198Erstellt: 27. Oktober 2026

Sodium Carbonate → 2,4'-Difluoro-6-nitro-1,1'-biphenyl

https://huagongshe.com/reaction/1776198

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktSodium HydroxideHCID 14798—
Edukt2-Chloro-1-fluoro-3-nitrobenzeneHCID 88883—
Edukt4-Fluorophenylboronic acidHCID 285645—
KatalysatorTetrabutylammonium BromideHCID 74236—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2,4'-Difluoro-6-nitro-1,1'-biphenylHCID 4631261257,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A microwave reaction vessel was charged with 2-chloro-3-fluoronitrobenzene (1.500 g, 8.5 mmol), 4-fluorophenylboronic acid (1.315 g, 9.4 mmol), sodium carbonate (2.717 g, 25.6 mmol), palladium diacetate (0.077 g, 0.3 mmol), tetrabutylammonium bromide (2.755 g, 8.5 mmol) in water (10 mL) and 1,4-dioxane (1 mL). The mixture was heated to 100° C. in a microwave reactor for 1 hr. The reaction was cooled to room temperature and poured into diethyl ether and 0.1N aqueous sodium hydroxide. The organic layer was washed with saturated aqueous sodium chloride, dried (anhydrous sodium sulfate), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (10-30% methylene chloride/hexanes) to give the desired product as a yellow solid (1.15 g, 57%). 1H NMR (CDCl3, 300 MHz) δ 7.70 (dt, 1H, J=8.4, 1.5 Hz), 7.51 (td, 1H, J=8.4, 5.4 Hz), 7.41 (td, 1H, J=8.4, 1.2 Hz), 7.35-7.26 (m, 2H), 7.22-7.11 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09265772B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-268505bdae854de2b3dbc106dcb9d4d4
Quellennotizuspto-grants-2016_02