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Ammonium Acetate → 1-Amino-5-(5-chloro-2-fluorophenyl)cyclohexan-3-one

HRID 1700702
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1700702
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([F:16])=[C:6]([CH:8]2[CH2:13][C:12](=O)[CH2:11][C:10](=[O:15])[CH2:9]2)[CH:7]=1.C([O-])(=O)C.[NH4+:21]>C(O)C>[NH2:21][CH:12]1[CH2:13][CH:8]([C:6]2[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[F:16])[CH2:9][C:10](=[O:15])[CH2:11]1
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Komponenten

4

Edukt 2

HCID 517165Ammonium AcetateHCID 183175245-(5-Chloro-2-fluorophenyl)cyclohexane-1,3-dione

Produkt 1

HCID 183173031-Amino-5-(5-chloro-2-fluorophenyl)cyclohexan-3-oneAusbeute 72,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A solution of 5-(5-chloro-2-fluorophenyl)cyclohexane-1,3-dione (2 g) and ammonium acetate (1.9 g) in ethanol (15 ml) was refluxed for 15 hours. The reaction solution was concentrated under reduced pressure, and to the residue were added water (30 ml) and ethyl acetate (150 ml). The mixture was shaken, and the separated upper layer was washed with water and concentrated under reduced pressure. The residue was washed with ethyl acetate and dried to give 1-amino-5-(5-chloro-2-fluorophenyl)cyclohexan-3-one (1.45 g) as yellow crystals.

Aufarbeitung

  1. concentrationThe reaction solution was concentrated under reduced pressure
  2. additionto the residue were added water (30 ml) and ethyl acetate (150 ml)
  3. washthe separated upper layer was washed with water
  4. concentrationconcentrated under reduced pressure
  5. washThe residue was washed with ethyl acetate
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-72ae725777ab457b997cae867f223b74
Quelldatensatz
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06350749B1

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