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Hydroxylamine → 1-[4-(4-Chloro-2-fluoro-phenoxy)-phenyl]-ethanone-oxime

HRID 1406332
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1406332
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13](=O)[CH3:14])=[CH:9][CH:8]=2)=[C:4]([F:18])[CH:3]=1.[NH2:19][OH:20]>C(O)C>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13](=[N:19][OH:20])[CH3:14])=[CH:9][CH:8]=2)=[C:4]([F:18])[CH:3]=1
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Komponenten

4

Edukt 2

HCID 787HydroxylamineHCID 667903211-(4-(4-Chloro-2-fluorophenoxy)phenyl)ethanone

Produkt 1

HCID 866588121-[4-(4-Chloro-2-fluoro-phenoxy)-phenyl]-ethanone-oxime

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of 3.4 g (12.8 mmol) of 1-[4-(4-chloro-2-fluoro-phenoxy)-phenyl]-ethanone and 3.0 mL hydroxylamine solution (50% in water) in 100 mL ethanol was refluxed for five hours. Then the mixture was evaporated to dryness, the residue was combined with approx. 15 mL water and extracted three times with 10 mL ethyl acetate. The extracts were washed with saturated sodium chloride solution, dried and evaporated down. The product thus obtained was reacted further without any further purification.

Aufarbeitung

  1. temperaturewas refluxed for five hours
  2. customThen the mixture was evaporated to dryness
  3. extractionextracted three times with 10 mL ethyl acetate
  4. washThe extracts were washed with saturated sodium chloride solution
  5. customdried
  6. customevaporated down
  7. customThe product thus obtained
  8. customwas reacted further without any further purification

Quellen und Nachweise

ORD-Eintrag
ord-e4b5dc36bc5c41c088d3f3b12c768717
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08916589B2

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