2,5-Dichlorophenol → 1-(2,5-Dichloro-phenoxy)-2-fluoro-4-nitro-benzene

HRID 33758

Reaktionsgleichung

Reaktionsgleichung von HRID 33758
[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[CH:5]=[CH:6][C:7]=1F.[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[OH:20].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[O:20][C:7]1[CH:6]=[CH:5][C:4]([N+:9]([O-:11])=[O:10])=[CH:3][C:2]=1[F:1]

Komponenten

5

Edukt 3

HCID 662,5-DichlorophenolHCID 11430Potassium CarbonateHCID 1230531,2-Difluoro-4-nitrobenzene

Produkt 1

HCID 597980461-(2,5-Dichloro-phenoxy)-2-fluoro-4-nitro-benzeneAusbeute 94,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A mixture of 3,4-difluoronitrobenzene (3.2 g, 0.02 mol), 2,5-dichlorophenol (3.59 g, 0.022 mol), and potassium carbonate (3.0 g, 0.022 mol) in 25 ml of anhydrous DMF was heated to 150° C. with stirring overnight. After cooling to room temperature, the reaction mixture was poured into 500 ml of ice water and stirred for 30 min. The precipitates were collected by filtration, washed with water, and dried in vacuo to give 5.72 g (94.7%) of crude product.

Aufarbeitung

  1. temperatureAfter cooling to room temperature
  2. stirringstirred for 30 min
  3. filtrationThe precipitates were collected by filtration
  4. washwashed with water
  5. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-fafef133eb40479aaefe077d5315a767
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07429667B2

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