Ammonium Chloride → 4-[Hydroxy(4-methoxyphenyl)methyl]benzonitrile

HRID 363049ノート

反応式

HRID 363049 の反応式
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([C:7]([C:9]2[CH:16]=[CH:15][C:12]([C:13]#[N:14])=[CH:11][CH:10]=2)=[O:8])=[CH:5][CH:4]=1.[BH4-].[Na+].[Cl-].[NH4+]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]([OH:8])[C:9]2[CH:10]=[CH:11][C:12]([C:13]#[N:14])=[CH:15][CH:16]=2)=[CH:17][CH:18]=1

参加物

5

実験手順

To a suspension of 4-(4-methoxybenzoyl)benzonitrile 26-1 (J. Med. Chem. 1991, 34, 2768-2778) (0.783 g, 3.3 mmol) in ethanol (35 ml) under nitrogen cooled in an ice-bath was added sodium borohydride (0.250 g, 6.6 mmol). The mixture was stirred 4 h with ice-bath cooling. To the resulting solution was added saturated ammonium chloride solution (35 ml). The mixture was partially evaporated under reduced pressure, and the resulting aqueous mixture was extracted with ethyl acetate (2×100 ml). The combined organic fractions were washed with brine (50 ml), dried (sodium sulfate), and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with ethyl acetate/hexane (1:6 increasing to 1:3), to give product 26-2 as an oil.

後処理

  1. temperaturecooled in an ice-bath
  2. temperaturecooling
  3. customThe mixture was partially evaporated under reduced pressure
  4. extractionthe resulting aqueous mixture was extracted with ethyl acetate (2×100 ml)
  5. washThe combined organic fractions were washed with brine (50 ml)
  6. dry with materialdried (sodium sulfate)
  7. customthe solvent was evaporated under reduced pressure
  8. customThe residue was purified by flash column chromatography on silica gel
  9. washeluting with ethyl acetate/hexane (1:6 increasing to 1:3)

出典と根拠

ORDレコード
ord-6e1d016534724a41bb7df789afa80dfd
出典データセット
uspto-grants-1999_02
特許番号
US05872138

反応ノート

読み込み中…