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Butanal → N,N-Di(propan-2-yl)but-1-en-1-amine

HRID 1415784
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1415784
[CH:1](=O)[CH2:2][CH2:3][CH3:4].[CH:6]([NH:9][CH:10]([CH3:12])[CH3:11])([CH3:8])[CH3:7]>C1C=CC=CC=1>[CH:6]([N:9]([CH:1]=[CH:2][CH2:3][CH3:4])[CH:10]([CH3:12])[CH3:11])([CH3:8])[CH3:7]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 261ButanalHCID 7912Diisopropylamine

Produkt 1

HCID 53723651N,N-Di(propan-2-yl)but-1-en-1-amineAusbeute 65 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

6.25 ml (69.3 mmol) of butyraldehyde and 19.44 ml (139 mmol) of diisopropylamine were dissolved in 30 ml of benzene, and the mixture was heated under reflux, while removing the water produced, until the production of water stopped (about 15 hours). The solvent was then removed by distillation under reduced pressure, and the residue was distilled under atmospheric pressure. Those fractions of the distillate having a boiling point of from 140 to 160° C. were collected, to give 6.95 g of the title compound as a pale yellow oily substance (yield 65%).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. customwhile removing the water
  4. customproduced, until the production of water
  5. custom(about 15 hours)
  6. customThe solvent was then removed by distillation under reduced pressure
  7. distillationthe residue was distilled under atmospheric pressure
  8. customof from 140 to 160° C.
  9. customwere collected

Quellen und Nachweise

ORD-Eintrag
ord-6b344b900a96485781fcc3d6e5b58b84
Quelldatensatz
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05908858

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