HCID 22258810, compound → HCID 22258826, compound

HRID 412226Notes

Reaction equation

HRID 412226 reaction equation
[F:1][C:2]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=2)[C:3]=1[C:4](N(OC)C)=[O:5].[CH3:24][Mg]Br>O1CCCC1>[F:1][C:2]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH2:15][C:16]2[CH:17]=[CH:18][C:19]([O:22][CH3:23])=[CH:20][CH:21]=2)[C:3]=1[C:4](=[O:5])[CH3:24]

Participants

4

Procedure

To a cold (0° C.) solution of 2-fluoro-N-methoxy-6-[(4-methoxybenzyl)oxy]-N-methylbenzamide (6.926 g, 21.70 mmol) in tetrahydrofuran (10 mL) was added 1N methyl magnesium bromide in tetrahydrofuran (43.40 mL, 43.40 mmol). The reaction mixture was stirred at reflux for 4 hrs. After cooled to room temperature, the reaction mixture was quenched with saturated aqueous NaHCO3 solution, and extracted with ethyl acetate. The separated organic phase was washed with water and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica gel (hexane:ethyl acetate, 3/1) to give 1-{2-fluoro-6-[(4-methoxybenzyl)oxy]phenyl}ethanone as a pale yellow solid (1.21 g, yield; 20%).

Workup

  1. temperatureat reflux for 4 hrs
  2. customthe reaction mixture was quenched with saturated aqueous NaHCO3 solution
  3. extractionextracted with ethyl acetate
  4. washThe separated organic phase was washed with water and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting residue was purified by column chromatography on silica gel (hexane:ethyl acetate, 3/1)

Sources & evidence

ORD record
ord-a727e5737c384a6db6dfb774f81e86eb
Source dataset
uspto-grants-2003_05
Patent number
US06562811B1

Reaction notes

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