Sulfuric Acid → Ethyl 3-oxovalerate

HRID 568828Notes

Reaction equation

HRID 568828 reaction equation
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5]CC)=O.[Mg].[C:13](Cl)(=O)[CH2:14]C.S(=O)(=O)(O)O>C(O)C.C(OCC)C.C(Cl)(Cl)(Cl)Cl>[C:3]([CH2:2][C:1]([O:9][CH2:10][CH3:11])=[O:8])(=[O:5])[CH2:13][CH3:14]

Participants

8

Procedure

A solution of diethyl malonate (80 g.) in ethanol (40 ml.) was added dropwise over 20 minutes to a mixture of magnesium (12.5 g.), carbontetrachloride (0.5 ml.) and ethanol (12.5 ml.) and stirred at room temperature for 10 minutes. Diethyl ether was added dropwise to the solution and refluxed under heating for 30 minutes. To the solution was added dropwise a solution of propionyl chloride (49 g.) in diethyl ether (50 ml.) under cooling over 10 minutes, and the mixture was refluxed under heating for 30 minutes. 20% sulfuric acid (200 ml.) was added to the solution, and the diethyl ether layer was separated, washed with 10% sulfuric acid and water successively, dried over magnesium sulfate and then filtered. The filtrate was evaporated in vacuo. To the oily residue was added β-naphthalene sulfonic acid hydrate (8 g.) and the mixture was heated at 200° C. for 1 hr. After cooling, diethyl ether (100 ml.) was added to the mixture and washed with 10% aqueous sodium carbonate (100 ml.) three times. The aqueous layer was extracted with diethyl ether (100 ml.) five times, and the extract was washed with water, dried over magesium sulfate and then distilled under reduced pressure (24 mmHg). The distillate at 100° to 110° C. was collected and distilled again under reduced pressure (25 mmHg). The distillate at 97° to 99° C. was collected to give ethyl propionylacetate (19.8 g).

Workup

  1. temperaturerefluxed
  2. temperatureunder heating for 30 minutes
  3. temperatureunder cooling over 10 minutes
  4. temperaturethe mixture was refluxed
  5. temperatureunder heating for 30 minutes
  6. customthe diethyl ether layer was separated
  7. washwashed with 10% sulfuric acid and water successively
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. customThe filtrate was evaporated in vacuo
  11. additionTo the oily residue was added β-naphthalene sulfonic acid hydrate (8 g.)
  12. temperaturethe mixture was heated at 200° C. for 1 hr
  13. temperatureAfter cooling
  14. additiondiethyl ether (100 ml.) was added to the mixture
  15. washwashed with 10% aqueous sodium carbonate (100 ml.) three times
  16. extractionThe aqueous layer was extracted with diethyl ether (100 ml.) five times
  17. washthe extract was washed with water
  18. dry with materialdried over magesium sulfate
  19. distillationdistilled under reduced pressure (24 mmHg)
  20. distillationThe distillate at 100° to 110° C. was collected
  21. distillationdistilled again under reduced pressure (25 mmHg)
  22. distillationThe distillate at 97° to 99° C. was collected

Sources & evidence

ORD record
ord-8715b904f8ce463b9cca3f08e60b9083
Source dataset
uspto-grants-1988_03
Patent number
US04729991

Reaction notes

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