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Gamma-Butyrolactone → 1-(2H-1,3-Benzodioxol-5-yl)pyrrolidin-2-one

HRID 1388335
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1388335
[CH2:1]1[O:10][C:9]2[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=2[O:2]1.[C:11]1(=O)[O:15][CH2:14][CH2:13][CH2:12]1>>[O:10]1[C:9]2[CH:8]=[CH:7][C:5]([N:6]3[CH2:11][CH2:12][CH2:13][C:14]3=[O:15])=[CH:4][C:3]=2[O:2][CH2:1]1
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Komponenten

3

Edukt 2

HCID 7302Gamma-ButyrolactoneHCID 843101,3-Benzodioxol-5-amine

Produkt 1

HCID 130503821-(2H-1,3-Benzodioxol-5-yl)pyrrolidin-2-oneAusbeute 51 %

Versuchsvorschrift

A mixture of 3,4-(methylenedioxy)aniline (200 g, 1.46 mole) and γ-butyrolactone (225 ml) was heated (in a dry nitrogen atmosphere) with stirring in a 200° oil bath for 2 days. Product was isolated from the reaction mixture by distillation under reduced pressure (b.p. 156°, 33 μ). Product was filtered over Silica Gel 60 (Trade Name) eluting with ethylacetate. The eluant was concentrated and the crystalline product was collected and washed with ether and petroleum ether affording 1-(1,3-benzodioxol-5-yl)-2-pyrrolidinone (153.4 g; 51%), m.p. 89°-91° which was one spot on tlc analysis.

Aufarbeitung

  1. temperaturewas heated (in a dry nitrogen atmosphere)
  2. custom
Product was isolated from the reaction mixture by distillation under reduced pressure (b.p. 156°, 33 μ)
  • filtrationProduct was filtered over Silica Gel 60 (Trade Name)
  • washeluting with ethylacetate
  • concentrationThe eluant was concentrated
  • customthe crystalline product was collected
  • washwashed with ether and petroleum ether
  • Quellen und Nachweise

    ORD-Eintrag
    ord-8fd80c0602794eaf866397578b6cbd1e
    Quelldatensatz
    uspto-grants-1984_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04431662

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