Water → 2-Oxo-2-pyridin-3-ylethyl 2,2-dimethylpropanoate

HRID 1058111Notes

Reaction equation

HRID 1058111 reaction equation
[C:1]([OH:7])(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].C(=O)([O-])O.[Na+].Cl.Cl[CH2:15][C:16]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)=[O:17].O>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C1COCC1>[CH3:3][C:2]([CH3:5])([CH3:4])[C:1]([O:7][CH2:15][C:16](=[O:17])[C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)=[O:6]

Participants

7

Procedure

Pivalic acid (5.3 g, 52 mmol), 8.8 g (104 mmol) of sodium hydrogen carbonate and 0.84 g (2.6 mmol) of tetrabutylammonium bromide were added to a solution of 5.0 g (26 mmol) of 3- (2-chloroacetyl) pyridine hydrochloride in 80 ml of THF at room temperature, and the mixture was refluxed for 2 hours. Water (100 ml) was added to the reaction mixture and the resulting mixture was extracted three times with 100 ml of ethyl acetate. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and then dried over sodium sulfate. The solvent was distilled off under reduced pressure and the product was isolated and purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give 5.3 g (yield 92%) of the desired 2-oxo-2-pyridin-3-ylethyl 2,2-dimethylpropanoate.

Workup

  1. temperaturethe mixture was refluxed for 2 hours
  2. extractionthe resulting mixture was extracted three times with 100 ml of ethyl acetate
  3. washThe organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution
  4. dry with materialdried over sodium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe product was isolated
  7. custompurified by silica gel column chromatography (hexane:ethyl acetate=1:1)

Sources & evidence

ORD record
ord-2d3b44607df94cfbbe80004652460851
Source dataset
uspto-grants-2003_02
Patent number
US06515134B1

Reaction notes

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