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Ammonium Chloride → 4-amino-2-fluoro-N-methoxy-N-methylbenzamide

HRID 13419
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 13419
[Cl-].[NH4+:2].[F:3][C:4]1[CH:15]=[CH:14][CH:13]=[CH:12][C:5]=1[C:6]([N:8]([O:10][CH3:11])[CH3:9])=[O:7]>CO.O.[Fe]>[NH2:2][C:14]1[CH:13]=[CH:12][C:5]([C:6]([N:8]([O:10][CH3:11])[CH3:9])=[O:7])=[C:4]([F:3])[CH:15]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 25517Ammonium ChlorideHCID 183575562-fluoro-N-methoxy-N-methylbenzamide

Produkt 1

HCID 231456994-amino-2-fluoro-N-methoxy-N-methylbenzamide

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23925IronKatalysatorHCID 887MethanolLösungsmittelHCID 962Water
Lösungsmittel

Versuchsvorschrift

15.2 g of ammonium chloride and 8 g of iron powder were added to a suspension of 10.84 g of 2-fluoro-N-methoxy-N-methylbenzamide in 60 ml of methanol and 30 ml of water, and the reaction liquid was heated under reflux for 3 hours. The reaction liquid was filtered through Celite, and the solvent was evaporated away under reduced pressure. The resulting residue was diluted with ethyl acetate, washed with water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1 to 1/2 to obtain the entitled compound as a brown oily substance.

Aufarbeitung

  1. customthe reaction liquid
  2. temperaturewas heated
  3. temperatureunder reflux for 3 hours
  4. customThe reaction liquid
  5. filtrationwas filtered through Celite
  6. customthe solvent was evaporated away under reduced pressure
  7. additionThe resulting residue was diluted with ethyl acetate
  8. washwashed with water
  9. dry with materialdried with anhydrous magnesium sulfate
  10. customThe solvent was evaporated away under reduced pressure
  11. customthe resulting residue was purified through silica gel column chromatography (
  12. customhexane/ethyl acetate=9/1 to 1/2 to obtain the entitled compound as a brown oily substance

Quellen und Nachweise

ORD-Eintrag
ord-5f7d2768bf7e4062b30e215939d2ca76
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07728025B2

Notizen zur Reaktion

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