1-(2,6-Dimethoxyphenyl)ethanone → Ethyl 4-(2,6-dimethoxyphenyl)-4-oxido-2-oxo-3-butenoate potassium salt

HRID 1585276

Reaktionsgleichung

Reaktionsgleichung von HRID 1585276
CC([O-])(C)C.[K+:6].[CH3:7][C:8]([C:10]1[C:15]([O:16][CH3:17])=[CH:14][CH:13]=[CH:12][C:11]=1[O:18][CH3:19])=[O:9].[C:20]([O:25][CH2:26][CH3:27])(=[O:24])[C:21]([O-])=[O:22]>C(O)C>[K+:6].[CH3:19][O:18][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]([O:16][CH3:17])[C:10]=1[C:8]([O-:9])=[CH:7][C:21](=[O:22])[C:20]([O:25][CH2:26][CH3:27])=[O:24]

Komponenten

5

Edukt 3

HCID 162671-(2,6-Dimethoxyphenyl)ethanoneHCID 21943339Ethanedioic acid, monoethyl esterHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 70244972Ethyl 4-(2,6-dimethoxyphenyl)-4-oxido-2-oxo-3-butenoate potassium salt

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

A solution of 13.4 g of 95% potassium tert-butylate in 72 ml of ethanol is added over 6 minutes to a solution, stirred and heated to 50° C., of 18 g of 2,6-dimethoxyacetophenone in 54 ml of ethanol. The mixture is heated to reflux, 16.3 ml of ethyl oxalate are added over 9 minutes and refluxing is continued for 1 hour. 40 ml of ethanol are then distilled off and the mixture is allowed to cool with stirring for two and a half hours. The mixture is filtered, and the precipitate is washed with 40 ml of ethanol and dried under vacuum at 60° C. for 17 hours to obtain 31 g of expected product.

Aufarbeitung

  1. temperatureThe mixture is heated
  2. temperatureto reflux
  3. temperaturerefluxing
  4. distillation40 ml of ethanol are then distilled off
  5. temperatureto cool
  6. stirringwith stirring for two and a half hours
  7. filtrationThe mixture is filtered
  8. washthe precipitate is washed with 40 ml of ethanol
  9. customdried under vacuum at 60° C. for 17 hours

Quellen und Nachweise

ORD-Eintrag
ord-e819e4d99e9146b7bb72c1362a935ada
Quelldatensatz
uspto-grants-1999_08
Patentnummer
US05936123

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