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Ammonium Chloride → 4-Chloro-5-iodobenzene-1,2-diamine

HRID 340764
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 340764
[Cl:1][C:2]1[C:3]([I:12])=[CH:4][C:5]([N+:9]([O-])=O)=[C:6]([CH:8]=1)[NH2:7].[NH4+].[Cl-]>CCO.O.[Fe]>[Cl:1][C:2]1[CH:8]=[C:6]([NH2:7])[C:5]([NH2:9])=[CH:4][C:3]=1[I:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 25517Ammonium Chloride2×HCID 223175485-Chloro-4-iodo-2-nitroaniline

Produkt 1

HCID 574814674-Chloro-5-iodobenzene-1,2-diamine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23925IronKatalysator2×HCID 702EthanolLösungsmittelHCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a suspension of 5-chloro-4-iodo-2-nitroaniline (36.5 g, 122 mmol) in EtOH (800 mL) and water (150 mL) was added iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol). The mixture was heated under nitrogen at 50° C. overnight. Additional iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol) were added and heating was continued for 45 h. The reaction mixture was cooled, filtered and concentrated. The resulting residue was re-dissolved in ethyl acetate and washed with sodium bicarbonate solution. The organic phase was concentrated to afford the desired product as a gray solid, which was used in the next step without further purification.

Aufarbeitung

  1. temperatureheating
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered
  4. concentrationconcentrated
  5. dissolutionThe resulting residue was re-dissolved in ethyl acetate
  6. washwashed with sodium bicarbonate solution
  7. concentrationThe organic phase was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-ca4ef106e17047ae8e06ce1b93002fad
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08895596B2

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