Iodobenzene → 2-Nitro-biphenyl-4-carboxylic acid methyl ester

HRID 2358804

Reaktionsgleichung

Reaktionsgleichung von HRID 2358804
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7](Br)=[C:6]([N+:11]([O-:13])=[O:12])[CH:5]=1.I[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>ClCCl.[Cu]>[CH3:1][O:2][C:3]([C:4]1[CH:9]=[CH:8][C:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[C:6]([N+:11]([O-:13])=[O:12])[CH:5]=1)=[O:14]

Komponenten

5

Reaktionsbedingungen

Temperatur
218 °C

Versuchsvorschrift

The product from Example 212a (0.100 g, 0.384 mmol) was combined with iodobenzene (0.375 mL, 3.35 mmol) and copper powder (0.188 g, 2.96 mmol) and the mixture heated in a sealed tube to 218° C. for 90 minutes. The reaction mixture was subsequently diluted with dichloromethane and filtered through celite. The crude product, obtained by concentration under vacuum, was purified by flash chromatography on silica gel (ethyl acetate-hexanes) to give the title compound (0.0847 g, 86

Aufarbeitung

  1. filtrationfiltered through celite
  2. customThe crude product, obtained by concentration under vacuum
  3. customwas purified by flash chromatography on silica gel (ethyl acetate-hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-6577f319bed74a60b3ccd62ec09a1ce4
Quelldatensatz
uspto-grants-2010_07
Patentnummer
US07763731B2

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