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Ethylenediamine → (2-Aminoethyl)[5-(trifluoromethyl)(2-pyridyl)]amine

HRID 31751
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 31751
Cl[C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][N:3]=1.[CH2:12]([NH2:15])[CH2:13][NH2:14]>>[NH2:14][CH2:13][CH2:12][NH:15][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][N:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 3301EthylenediamineHCID 923422-Chloro-5-(trifluoromethyl)pyridine

Produkt 1

HCID 2779424(2-Aminoethyl)[5-(trifluoromethyl)(2-pyridyl)]amine

Versuchsvorschrift

2-Chloro-5-(trifluoromethyl)pyridine (5.0 g) was heated with ethylenediamine (20 ml) at 120° C. overnight. The excess ethylenediamine was removed by rotary evaporation and the residue was partitioned between dichloromethane and 2.5 M aqueous sodium hydroxide. The aqueous layer was extracted 5 times further with dichloromethane. The combined organic layers were washed with a saturated aqueous sodium chloride solution, dried, then concentrated in vacuo to give (2-aminoethyl)[5-(trifluoromethyl)(2-pyridyl)]amine as an orange oil.

Aufarbeitung

  1. customThe excess ethylenediamine was removed by rotary evaporation
  2. customthe residue was partitioned between dichloromethane and 2.5 M aqueous sodium hydroxide
  • extractionThe aqueous layer was extracted 5 times further with dichloromethane
  • washThe combined organic layers were washed with a saturated aqueous sodium chloride solution
  • customdried
  • concentrationconcentrated in vacuo
  • Quellen und Nachweise

    ORD-Eintrag
    ord-c90571fea176455db5acc4975a90b2f6
    Quelldatensatz
    uspto-grants-2008_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US07425557B2

    Notizen zur Reaktion

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