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Hydrochloric Acid → 2-(3,5-Dioxo-1,2,4-triazolidin-4-yl)acetic acid

HRID 1660121
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1660121
[O:1]=[C:2]1[N:6]([CH2:7][C:8]([O:10]C)=[O:9])[C:5](=[O:12])[NH:4][NH:3]1.[OH-].[Na+].Cl>>[O:1]=[C:2]1[N:6]([CH2:7][C:8]([OH:10])=[O:9])[C:5](=[O:12])[NH:4][NH:3]1
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Komponenten

4

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 53759869Methyl 3,5-dioxo-1,2,4-triazolidine-4-acetate

Produkt 1

HCID 205575302-(3,5-Dioxo-1,2,4-triazolidin-4-yl)acetic acidAusbeute 33 %

Versuchsvorschrift

0.5 g (2.9 mmol) of methyl 3,5-dioxo-1,2,4-triazolidine-4-acetate was stirred at room temperature for 2 hours with 8.7 ml (8.7 mmol) of 1-M sodium hydroxide solution. The resulting solution was acidified with concentrated hydrochloric acid and evaporated to dryness. The solid residue was extracted with hot acetonitrile. The acetonitrile extracts were evaporated and the residual colourless solid was recrystallized from acetonitrile, there being obtained 0.15 g (33%) of 3,5-dioxo-1,2,4-triazolidine-4-acetic acid of melting point 220°-223° C. (from acetonitrile).

Aufarbeitung

  1. customevaporated to dryness
  2. extractionThe solid residue was extracted with hot acetonitrile
  3. customThe acetonitrile extracts were evaporated
  4. customthe residual colourless solid was recrystallized from acetonitrile, there

Quellen und Nachweise

ORD-Eintrag
ord-75b26e5952c944288a2a8754a147d2d3
Quelldatensatz
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04307094

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