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

HRID 1393137
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1393137
[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-2ad94dae1a3a44fb8f5a2eb2c5b22950
Quelldatensatz
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07345064B2

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