Potassium Iodide → Ethyl 2-benzoyl-4-oxopentanoate

HRID 413884Notes

Reaction equation

HRID 413884 reaction equation
C(=O)([O-])[O-].[K+].[K+].[C:7]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])(=[O:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[I-].[K+].Cl[CH2:24][C:25](=[O:27])[CH3:26]>CC(C)=O>[CH2:19]([O:18][C:16](=[O:17])[CH:15]([C:7](=[O:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH2:24][C:25](=[O:27])[CH3:26])[CH3:20]

Participants

6

Procedure

Potassium carbonate (200 mmol, 27.6 g) was added to a solution of ethyl benzoylacetate (100 mmol, 19.2 g) and potassium iodide (20 mmol, 3.3 g) in dry acetone (100 mL). The resulting solution was refluxed, and chloroacetone (110 mmol, 10.7 g) was added dropwise. Analysis of the reaction mixture by GC/MS indicated the presence of Intermediate 2. Solid material was filtered from the reaction mixture, then washed with 200 mL acetone. The resulting filtrate was concentrated under vacuum, redissolved in ether, then washed three times with water (100 mL). The organic layer was separated from the aqueous layer, and dried over MgSO4. The solids were separated, and the organic solvents removed under vacuum to yield a yellow/orange oil. The crude oil was purified by Kugelrohr distillation (b.p. 175-185 at 0.65 Torr.).

Workup

  1. temperatureThe resulting solution was refluxed
  2. filtrationSolid material was filtered from the reaction mixture
  3. washwashed with 200 mL acetone
  4. concentrationThe resulting filtrate was concentrated under vacuum
  5. dissolutionredissolved in ether
  6. washwashed three times with water (100 mL)
  7. customThe organic layer was separated from the aqueous layer
  8. dry with materialdried over MgSO4
  9. customThe solids were separated
  10. customthe organic solvents removed under vacuum
  11. customto yield a yellow/orange oil
  12. distillationThe crude oil was purified by Kugelrohr distillation (b.p. 175-185 at 0.65 Torr.)

Sources & evidence

ORD record
ord-6d626667149f4450b542f494fa171142
Source dataset
uspto-grants-2003_05
Patent number
US06569890B2

Reaction notes

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