Acetic Acid → Ethyl 2-oxocyclopentanecarboxylate

HRID 1964786Notes

Reaction equation

HRID 1964786 reaction equation
[Na].[C:2]([O:13]CC)(=O)[CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8].C(O)(=O)C>C1(C)C=CC=CC=1>[CH3:11][CH2:10][O:9][C:7]([CH:6]1[C:2](=[O:13])[CH2:3][CH2:4][CH2:5]1)=[O:8]

Participants

5

Procedure

15.0 g (0.652 mmol) of sodium was placed in 150 mL toluene, heated to reflux, shaken, and made into sodium sand. 81.6 g (0.400 mol) of diethyl adipate was added in drops to the mixture in an outside bath at 105-110° C., and the resultant solution changed into a yellow sticky product. After refluxing for 8 h, the solution was cooled by ice bath, and 400 mL of 10% acetic acid solution was added in drops. The mixture was suction filtered and washed with a small amount of toluene. The filtrate was separated into layers. The upper layer was washed with 7% sodium carbonate (260 mL×2) followed by saturated brine (200 mL×2), and dried overnight with anhydrous magnesium sulfate. The solution was filtered, concentrated and distilled under reduced pressure to collect the fractions of bp: 142-150° C./2660 Pa, yielding 53.3 g of colorless liquid with a yield of 85.6%.

Workup

  1. temperatureheated
  2. temperatureto reflux
  3. temperatureAfter refluxing for 8 h
  4. temperaturethe solution was cooled by ice bath
  5. filtrationfiltered
  6. washwashed with a small amount of toluene
  7. customThe filtrate was separated into layers
  8. washThe upper layer was washed with 7% sodium carbonate (260 mL×2)
  9. dry with materialdried overnight with anhydrous magnesium sulfate
  10. filtrationThe solution was filtered
  11. concentrationconcentrated
  12. distillationdistilled under reduced pressure
  13. customto collect the fractions of bp: 142-150° C./2660 Pa

Sources & evidence

ORD record
ord-1c7a681f39ad429ca198d33877710219
Source dataset
uspto-grants-2013_04
Patent number
US08415505B2

Reaction notes

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