Diethyl Oxalate → Diethyl 2-butyl-3-oxobutanedioate

HRID 398987

Reaktionsgleichung

Reaktionsgleichung von HRID 398987
[C:1]([O:8][CH2:9][CH3:10])(=[O:7])[C:2]([O:4]CC)=O.CC[O-].[Na+].[Na].[C:16]([O:23][CH2:24][CH3:25])(=[O:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]>O.C(O)C.CCOCC>[CH2:18]([CH:17]([C:2](=[O:4])[C:1]([O:8][CH2:9][CH3:10])=[O:7])[C:16]([O:23][CH2:24][CH3:25])=[O:22])[CH2:19][CH2:20][CH3:21]

Komponenten

8

Versuchsvorschrift

100 ml of ether, then 13.55 ml of diethyl oxalate were added to a solution of sodium ethylate prepared by stirring 2.3 g of sodium and 150 ml of ethanol at 40° C. for one hour. The mixture was refluxed for 15 minutes, cooled down slightly and 50 ml of ethyl caproate were added. The mixture was stirred at reflux for 3 hours and at 30° C. to 35° C. for 16 hours. 50 ml of water were added and the aqueous phase was separated by decanting, washed twice with ether and acidified with 2N hydrochloric acid. Extraction was carried out 3 times with ether and the combined organic phases were washed with water, then with a saturated solution of sodium chloride, dried and evaporated to dryness to obtain 9.5 g of the desired product which was used as is for the following step.

Aufarbeitung

  1. customprepared
  2. temperatureThe mixture was refluxed for 15 minutes
  3. temperaturecooled down slightly
  4. temperatureat reflux for 3 hours and at 30° C. to 35° C. for 16 hours
  5. customthe aqueous phase was separated
  6. customby decanting
  7. washwashed twice with ether
  8. extractionExtraction
  9. washthe combined organic phases were washed with water
  10. dry with materialwith a saturated solution of sodium chloride, dried
  11. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-88d0b947f0114e4dae17c9002676060a
Quelldatensatz
uspto-grants-1998_10
Patentnummer
US05817674

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