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Methyl Acrylate → 3-[(2-Methoxycarbonyl-ethyl)-methyl-amino]-butyric acid methyl ester

HRID 480249
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 480249
[CH3:1][O:2][C:3](=[O:9])[CH2:4][CH:5]([NH:7][CH3:8])[CH3:6].[C:10]([O:14][CH3:15])(=[O:13])[CH:11]=[CH2:12]>>[CH3:1][O:2][C:3](=[O:9])[CH2:4][CH:5]([N:7]([CH2:12][CH2:11][C:10]([O:14][CH3:15])=[O:13])[CH3:8])[CH3:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 7294Methyl AcrylateHCID 12636115Methyl 3-(methylamino)butanoate

Produkt 1

HCID 220914183-[(2-Methoxycarbonyl-ethyl)-methyl-amino]-butyric acid methyl esterAusbeute 58 %

Versuchsvorschrift

3-Methylamino-butyric acid methyl ester (7.6 g, 58 mmol, 1.0 equiv) was added neat to methyl acrylate (7.5 g, 87 mmol, 1.5 equiv). The resulting solution was refluxed for 16 h. The reaction was cooled and diluted with hexanes (200 mL) and an insoluble polymer separated out. The hexane solution was decanted and the polymer was washed 2×100 mL hexanes with vigorous stirring. The combined hexane solutions were then concentrated in vacuo. The crude product was purified by flash chromatography on SiO2 using pure CH2Cl2 as an eluent. The pure product was isolated as a clear colorless oil (7.3 g, 58%); MS, m/z 218=M+1.

Aufarbeitung

temperature
The resulting solution was refluxed for 16 h
  • temperatureThe reaction was cooled
  • customan insoluble polymer separated out
  • customThe hexane solution was decanted
  • washthe polymer was washed 2×100 mL hexanes with vigorous stirring
  • concentrationThe combined hexane solutions were then concentrated in vacuo
  • customThe crude product was purified by flash chromatography on SiO2 using pure CH2Cl2 as an eluent
  • Quellen und Nachweise

    ORD-Eintrag
    ord-5fd3f10cf11e483eb4ec35b3441b465a
    Quelldatensatz
    uspto-grants-2003_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06649642B2

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