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Ethyl 2,4-dioxovalerate → 4-Acetyl-3-hydroxy-1H-pyrrol-2(5H)-one

HRID 234724
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 234724
[O:1]=[C:2]([CH2:8][C:9](=[O:11])[CH3:10])[C:3]([O:5]CC)=O.[Cl-].C[C:14](=[NH2+:16])C>C(#N)C>[C:9]([C:8]1[CH2:14][NH:16][C:3](=[O:5])[C:2]=1[OH:1])(=[O:11])[CH3:10]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 69208Ethyl 2,4-dioxovalerateHCID 21939857Dimethylmethyleneammonium chloride

Produkt 1

HCID 233554434-Acetyl-3-hydroxy-1H-pyrrol-2(5H)-oneAusbeute 33,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
-40 °C

Versuchsvorschrift

A solution of ethyl 2,4-dioxovalerate (1.13 g, 7.11 mmole), dimethylmethylene ammonium chloride (0.67 g, 7.11 mmole) and acetonitrile (3 ml) was stirred at 25° C. over 45 minutes. The resulting yellow homogeneous solution was then cooled to -40° C. and ammonia gas was bubbled through the mixture over 5 minutes, during which time a yellow solid precipitated out of solution. The stirred mixture was allowed to slowly warm to 5° C. over a period of 1 hour before addition of concentrated ammonium hydroxide (4 ml). After stirring for 1 hour, the mixture was concentrated under reduced pressure, diluted with 3N HCl (6 ml) and extracted with ethyl acetate (50 ml×10). The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to give 0.34 g of the title compound as a yellow amorphous solid. M.P. 178°-180° C. (dec); 1H nmr (250 MHz, DMSO-d6) δ2.42 (s, 3H), 3.78 (s, 2H), 8.87 (s, 1H); Anal. calcd. for C6H7NO3 : C, 51.07; H, 5.00; N, 9.92. Found: C, 51.18; H, 5.23; N, 9.73.

Aufarbeitung

  1. customammonia gas was bubbled through the mixture over 5 minutes, during which time a yellow solid
  2. customprecipitated out of solution
  3. temperatureto slowly warm to 5° C. over a period of 1 hour before addition of concentrated ammonium hydroxide (4 ml)
  4. concentrationthe mixture was concentrated under reduced pressure
  5. additiondiluted with 3N HCl (6 ml)
  6. extractionextracted with ethyl acetate (50 ml×10)
  7. dry with materialThe combined organics were dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-08f430d91fcc4836ba383269365fd0ff
Quelldatensatz
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05596013

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