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5-Fluoroindanone oxime → 5-Fluoro-2,3-dihydro-1H-inden-1-amine

HRID 375600
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 375600
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[N:11]O)[CH2:6][CH2:5]2>C(O)(=O)C.[Zn]>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH:7]([NH2:11])[CH2:6][CH2:5]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 736055205-Fluoroindanone oxime

Produkt 1

HCID 166663285-Fluoro-2,3-dihydro-1H-inden-1-amineAusbeute 96,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

Zinc powder (20.2 g) was added during three hours to the stirred solution of the above oxime (20.2 g) in acetic acid (200 ml) which maintains the temperature at 25°-35° C. The resulting mixture was stirred an additional 12 hours at room temperature. The solids were removed by filtration and the filtrate concentrated in vacuo. The concentrated filtrate was partitioned between water and toluene and the aqueous phase adjusted to pH 12 with ammonium hydroxide and extracted with toluene. Solvent removal in vacuo gave 5-fluoro-1-aminoindan (17.8 g) as a colored oil.

Aufarbeitung

  1. customat 25°-35° C
  2. customThe solids were removed by filtration
  3. concentrationthe filtrate concentrated in vacuo
  4. customThe concentrated filtrate was partitioned between water and toluene
  5. extractionextracted with toluene
  6. customSolvent removal in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-308f788b92cc49588ca4ad24af84b0b0
Quelldatensatz
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05486541

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