Allylamine → HCID 4153372, Verbindung
Reaktionsgleichung
[C:1](Cl)(=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[CH2:9]([NH2:12])[CH:10]=[CH2:11]>O1CCCC1>[CH2:9]([NH:12][C:1](=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[CH:10]=[CH2:11]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 15 °C
Versuchsvorschrift
Hexanoyl chloride (33 g, 0.25 mol) in 250 mL of tetrahydrofuran was added to a three neck round bottom flask equipped with a thermometer, stir bar, and dropping funnel. The contents of the flask were then cooled to 15° C. in an ice bath while stirring. Allylamine (28.6 g 0.5 mol) in 200 mL of tetrahydrofuran was then added slowly through the dropping funnel while maintaining stirring. Throughout the addition, the temperature was maintained at 15° C. After addition was complete, stirring continued for an additional 15 minutes, after which the solid allylamine chloride precipitate was filtered off. The filtration was concentrated under vacuum to yield 37 g of N-allyl hexanamide as a colorless viscous liquid.
Aufarbeitung
- customequipped with a thermometer
- stirringwhile stirring
- temperaturewhile maintaining
- stirringstirring
- additionThroughout the addition
- temperaturethe temperature was maintained at 15° C
- additionAfter addition
- stirringstirring
- filtrationafter which the solid allylamine chloride precipitate was filtered off
- filtrationThe filtration
- concentrationwas concentrated under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-d2ef61e5f5434733959ebae7490fc8d4
- Quelldatensatz
- uspto-grants-2003_08
- Patentnummer
- US06605270B1
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