Potassium Chloride → HCID 178472876, Verbindung

HRID 358028

Reaktionsgleichung

Reaktionsgleichung von HRID 358028
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[N:10]([O-])=[O:11].[Na+].[Cl-].[K+]>C(O)(=O)C.O>[OH:11]/[N:10]=[C:2](/[C:3](=[O:4])[CH3:5])\[C:1]([O:7][CH2:8][CH3:9])=[O:6]

Komponenten

6

Edukt 3

HCID 4873Potassium ChlorideHCID 8868Ethyl AcetoacetateHCID 23668193Sodium Nitrite

Produkt 1

HCID 178472876HCID 178472876, VerbindungAusbeute 86,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittelHCID 962WaterLösungsmittel2×

Versuchsvorschrift

To a stirred and ice-cooled solution of ethyl acetoacetate (292 g) in glacial acetic acid (296 ml) was added a solution of sodium nitrite (180 g) in water (400 ml) at such a rate that the reaction temperature was maintained below 10° C. Stirring and cooling were continued for about 30 min, when a solution of potassium chloride (160 g) in water (800 ml) was added. The resulting mixture was stirred for one hour. The lower oily phase was separated and the aqueous phase was extracted with diethyl ether. The extract was combined with the oil, washed successively with water and saturated brine, dried, and evaporated. The residual oil, which solidified on standing, was washed with petrol and dried in vacuo over potassium hydroxide, giving ethyl (Z)-2-(hydroxyimino)-3-oxobutyrate (309 g).

Aufarbeitung

  1. temperaturewas maintained below 10° C
  2. stirringStirring
  3. temperaturecooling
  4. stirringThe resulting mixture was stirred for one hour
  5. customThe lower oily phase was separated
  6. extractionthe aqueous phase was extracted with diethyl ether
  7. washwashed successively with water and saturated brine
  8. customdried
  9. customevaporated
  10. washwas washed with petrol
  11. dry with materialdried in vacuo over potassium hydroxide

Quellen und Nachweise

ORD-Eintrag
ord-3108ea06fe3140c587b3f4e659608279
Quelldatensatz
uspto-grants-1984_08
Patentnummer
US04464368

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