StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

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

HRID 18379
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 18379
[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 the resulting insoluble matter was filtered out, and the filtrate was concentrated under reduced pressure. Chloroform (1 L) and a 4 N aqueous sodium hydroxide solution (500 ml) were added to the resulting residue. After separation, the organic layer was dried over sodium sulfate and concentrated under reduced pressure. Then the obtained concentrate was distilled under reduced pressure to give the target compound (20.5 g, 60%) as a colorless oily matter.

Aufarbeitung

  1. temperaturethe mixture was refluxed for three hours
  2. filtrationthe resulting insoluble matter was filtered out
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. additionChloroform (1 L) and a 4 N aqueous sodium hydroxide solution (500 ml) were added to the resulting residue
  5. customAfter separation
  6. dry with materialthe organic layer was dried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. concentrationThen the obtained concentrate
  9. distillationwas distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-900edad9764d45058c5a034c2883b05b
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07741346B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion