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Hydrazine hydrate (1:1) → 3-(Pyridin-4-yl)propan-1-amine

HRID 11433
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 11433
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9][N:10]2C(=O)C3=CC=CC=C3C2=O)=[CH:3][CH:2]=1.O.NN>CO>[NH2:10][CH2:9][CH2:8][CH2:7][C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24654Hydrazine hydrate (1:1)HCID 12015796N-[3-(4-Pyridyl)propyl]phthalimide

Produkt 1

HCID 143474663-(Pyridin-4-yl)propan-1-amineAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

N-[3-(4-Pyridyl)propyl]phthalimide (67.1 g, 252 mmol) was mixed with methanol (504 ml) and hydrazine monohydrate (18.3 ml, 378 mmol), and the mixture was refluxed for three hours. The reaction mixture was allowed to stand, then an insoluble matter was filtered out, and the filtrate was concentrated under reduced pressure. Chloroform (1 liter) and a 4 N aqueous sodium hydroxide solution (500 ml) were added to the residue, layers were separated, and the organic layer was dried over sodium sulfate. The organic layer was concentrated under reduced pressure and then distilled under reduced pressure to give 20.5 g (60%) of the titled compound as a colorless oily matter.

Aufarbeitung

  1. temperaturethe mixture was refluxed for three hours
  2. filtrationan insoluble matter was filtered out
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. additionChloroform (1 liter) and a 4 N aqueous sodium hydroxide solution (500 ml) were added to the residue, layers
  5. customwere separated
  6. dry with materialthe organic layer was dried over sodium sulfate
  7. concentrationThe organic layer was concentrated under reduced pressure
  8. distillationdistilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-32b25cabc2204a3c84c6a781a1d54418
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07098226B2

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