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Methyl iodide → N-[2-(2-methoxyethoxy)ethyl]acrylamide

HRID 2054571
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2054571
[OH:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][NH:7][C:8](=[O:11])[CH:9]=[CH2:10].[OH-].[K+].[CH3:14]I>O1CCCC1>[CH3:14][O:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][NH:7][C:8](=[O:11])[CH:9]=[CH2:10]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 19364541HCID 19364541, Verbindung

Produkt 1

HCID 61849582N-[2-(2-methoxyethoxy)ethyl]acrylamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

N-[2-(2-hydroxyethoxy)ethyl]acrylamide (35.87 g), potassium hydroxide (15.2 g), tetrahydrofuran (100 g) and methyl iodide (33.58 g) were introduced into a 1 L eggplant type flask equipped with a reflux condenser and a magnetic rotor. A reaction was carried out at 45° C. for 2 hours and then for 2 hours at 60° C. as the mixture was being stirred. The salt that separated out was removed by filtration and the low boiling point components were removed by means of a rotary vacuum evaporator. Purification was performed by distillation under reduced pressure and N-[2-(2-methoxyethoxy)ethyl]acrylamide was obtained as a yellow transparent, viscous liquid.

Aufarbeitung

  1. customequipped with a reflux condenser
  2. customThe salt that separated out
  3. customwas removed by filtration
  4. customthe low boiling point components were removed by means of a rotary vacuum evaporator
  5. customPurification
  6. distillationwas performed by distillation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3ed0b7e229d8429baa4f38b435f191b5
Quelldatensatz
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07329694B2

Notizen zur Reaktion

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