Nitric Acid → 4-(Pentafluoroethyl)-2-nitrophenol

HRID 884942Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 884942
[F:1][C:2]([F:14])([C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)[C:3]([F:6])([F:5])[F:4].S(=O)(=O)(O)O.[N+:20]([O-])([OH:22])=[O:21]>C(O)(=O)C>[F:1][C:2]([F:14])([C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([N+:20]([O-:22])=[O:21])[CH:8]=1)[C:3]([F:5])([F:4])[F:6]

Komponenten

5

Edukt 3

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 10856782Phenol, 4-(pentafluoroethyl)-

Produkt 1

HCID 866510624-(Pentafluoroethyl)-2-nitrophenolAusbeute 67,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel2×

Versuchsvorschrift

To a mixture of 1.70 g of 4-(pentafluoroethyl)phenol, 6 ml of acetic acid and 2.0 ml of concentrated sulfuric acid, a mixture of 0.80 g of 69% nitric acid and 1 ml of acetic acid was added dropwise while ice-cooling, and stirred at room temperature for three hours. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate three times. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 1.40 g of 4-(pentafluoroethyl)-2-nitrophenol.

Aufarbeitung

  1. additionwas added dropwise while ice-
  2. temperaturecooling
  3. extractionfollowed by extraction with ethyl acetate three times
  4. washThe combined organic layers were washed with water
  5. dry with materiala saturated sodium chloride solution, dried over sodium sulfate
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b2983bdbabe042b4a0d1f6b20cb615d9
Quelldatensatz
uspto-grants-2012_08
Patentnummer
US08242133B2

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