Sodium hydride → 4-[2-(N-Benzoyl-N-methylamino)ethoxy]benzaldehyde

HRID 2260709

反応式

HRID 2260709 の反応式
[H-].[Na+].[C:3]([N:11]([CH2:13][CH2:14][OH:15])[CH3:12])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.F[C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[O:22])=[CH:19][CH:18]=1>CN(C)C=O>[C:3]([N:11]([CH2:13][CH2:14][O:15][C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[O:22])=[CH:19][CH:18]=1)[CH3:12])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

参加物

5

実験手順

Sodium hydride (60% dispersion in oil, 1.30 g) was added portionwise to a solution of 2-(N-benzoyl-N-methylamino)ethanol (5.0 g) in dry dimethylformamide (100 ml) at room temperature under a nitrogen atmosphere. The mixture was stirred at room temperature for 1 hour prior to the addition of 4-fluorobenzaldehyde (5.09 g, 4.4 ml), and the mixture then heated at 80° C. for 15 hours. The solvent was evaporated and the residue dissolved in water (500 ml) and extracted with ethyl acetate (3×500 ml). The combined ethyl acetate layers were washed with water (2×300 ml), brine (300 ml), dried (MgSO4) and evaporated to yield an oil. The oil was triturated with hexane, and the residue chromatographed on silica gel with 1.5% methanol in dichloromethane to afford the title compound as an oil.

後処理

  1. temperaturethe mixture then heated at 80° C. for 15 hours
  2. customThe solvent was evaporated
  3. dissolutionthe residue dissolved in water (500 ml)
  4. extractionextracted with ethyl acetate (3×500 ml)
  5. washThe combined ethyl acetate layers were washed with water (2×300 ml), brine (300 ml)
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. customto yield an oil
  9. customThe oil was triturated with hexane
  10. customthe residue chromatographed on silica gel with 1.5% methanol in dichloromethane

出典と根拠

ORDレコード
ord-db686fe8ffe24339a2419a14a7183478
出典データセット
uspto-grants-1995_12
特許番号
US05478851

関連ノート

読み込み中…