Sodium Hydroxide → HCID 85865899、化合物

HRID 1296706ノート

反応式

HRID 1296706 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:8](O)=[CH:9][C:10]2[CH:15]=[CH:14][N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][CH:7]=1.Cl.[NH2:18][OH:19].[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([C:8](=[N:18][OH:19])[CH2:9][C:10]2[CH:15]=[CH:14][N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][CH:7]=1

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 1363756171-(3-Chlorophenyl)-2-(4-pyrimidinyl)ethenol

生成物 1

HCID 85865899HCID 85865899、化合物収率 68%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a suspension of 1-(3-chlorophenyl)-2-(4-pyrimidinyl)ethenol (9.0 g, 38.7 mmol) in methanol (100 mL) was added hydroxylamine hydrochloride (11.5 g, 165 mmol) and sodium hydroxide (60 mL, 2.8 M in water, 166 mmol). The reaction mixture was refluxed 4 hours. After cooling, the excess methanol was removed in vacuo. Ice water (˜300 mL) was added to the resultant mixture and the ice was allowed to melt. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, then dried over magnesium sulfate. Filtration and concentration followed by flash chromatography (3:1 to 2:1 hexanes:ethyl acetate) provided 1-(3-chlorophenyl)-2-(4-pyrimidinyl)ethanone oxime (6.5 g, 68%) as a white solid. Rf 0.14 (3:1 hexanes:ethyl acetate): 1H NMR (CDCl3) δ 9.50 (br, 1H), 9.18 (s, 1H), 8.61 (d, 1H), 7.78 (s, 1H), 7.58 (d, 1H), 7.38–7.25 (m, 3H), 4.38 (s, 2H); MS m/z 248 (M+1).

後処理

  1. temperatureThe reaction mixture was refluxed 4 hours
  2. temperatureAfter cooling
  3. customthe excess methanol was removed in vacuo
  4. additionIce water (˜300 mL) was added to the resultant mixture
  5. extractionThe aqueous mixture was extracted with ethyl acetate
  6. washThe organic layer was washed with water and brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationFiltration and concentration

出典と根拠

ORDレコード
ord-212f12a008c447358cda74e16177f6f8
出典データセット
uspto-grants-2007_07
特許番号
US07247626B2

反応ノート

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