Hydrochloric Acid → HCID 10846626, compound

HRID 2263583Notes

Reaction equation

HRID 2263583 reaction equation
[C:1]([CH2:9][CH2:10][C:11]([OH:13])=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.CC(C)(C)C(Cl)=O.[CH3:28][NH:29][O:30][CH3:31].Cl>ClCCl.O>[CH3:31][O:30][N:29]([CH3:28])[C:11]([CH2:10][CH2:9][C:1]([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:8])=[O:13]

Participants

8

Procedure

3-Benzoylpropionic acid (3.56 g, 20.0 mmol) was dissolved in dichloromethane (50 mL), to the solution was added triethylamine (2.22 g, 22.0 mmol) and trimethylacetyl chloride (2.41 g, 20.0 mmol) at 0° C., and the mixture was stirred at room temperature for 60 hours. Subsequently, to the reaction mixture was successively added triethylamine (4.04 g, 40.0 mmol) and N,O-dimethylhydroxylamine (1.95 g, 20.0 mmol), and the mixture was further stirred at room temperature for 5 hours. To the reaction mixture was added water and 1 mol/L hydrochloric acid, and the mixture was extracted with chloroform. The organic layer was washed with aqueous sodium hydrogencarbonate and water and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by column chromatography (chloroform/methanol=50/1→40/1) to give 3-(N-methoxy-N-methylcarbamoyl)-propiophenone (1.53 g, 35%).

Workup

  1. stirringthe mixture was further stirred at room temperature for 5 hours
  2. extractionthe mixture was extracted with chloroform
  3. washThe organic layer was washed with aqueous sodium hydrogencarbonate and water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe resulting residue was purified by column chromatography (chloroform/methanol=50/1→40/1)

Sources & evidence

ORD record
ord-3853b4decc5a4c74a259f09a9c4f0466
Source dataset
uspto-grants-2010_12
Patent number
US07851635B2

Reaction notes

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