Reaktion #85600

ord-6a5d8e0b4f2f48f6baff74346c1a6d6d

Reaktionsgleichung

O=c1n(Cl)c(=O)n(Cl)c(=O)n1Cl
TCCA
Cc1ccc(F)cc1[N+](=O)[O-]
4-fluoro-1-methyl-2-nitrobenzene
CC(=O)O.O=S(=O)(O)O
CH3CO2H H2SO4
Cc1ccc(O)c(O)c1
compound 1
Ausbeute 33.1%
Cc1ccc(O)c(O)c1
4-methylcatechol
Ausbeute 33.1%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling to room temperature
  2. 2
    Extraktionextracted with DCM (2×200 mL)
  3. 3
    WaschenThe combined organic phase was washed with brine
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    SonstigeThe residue was purified by column chromatography (PE: EA=50:1)

Vorschrift

TCCA (16.7 g, 72 mmol) was added to a solution of 4-fluoro-1-methyl-2-nitrobenzene (12.4 g, 80 mmol) in CH3CO2H/H2SO4 (80 mL/80 mL). The mixture was heated to 70° C. and stirred overnight. After cooling to room temperature, the reaction mixture was poured into ice water (1000 mL) and extracted with DCM (2×200 mL). The combined organic phase was washed with brine and concentrated in vacuo. The residue was purified by column chromatography (PE: EA=50:1) to give compound 1 (5.0 g, 33.1%) as a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434724B2uspto-grants-2016_09