反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH3:10])[N+:5]([O-])=[CH:6][C:7]=1[F:8].C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C.[Fe]>[Cl:1][C:2]1[C:7]([F:8])=[CH:6][N:5]=[C:4]([CH3:10])[CH:3]=1参加物
実験手順
4-Chloro-5-fluoro-2-picoline-N-oxide (12.43 g, 76.93 mmol), from Step 7, was dissolved in 52 mL of glacial acetic acid in a 3-necked flask equiped with a mechanical stirrer, a condenser and a thermometer. Iron powder (6.45 g, 115.5 mmol) was added to the solution at ambient temperature and the reaction mixture was carefully heated to 35°-40° C. After 10 min at 30° C., an exothermic reaction took place which caused the reaction temperature to rise to 120° C. and the reaction mixture became a very dark brown-colored solution. The flask was transferred to a cold water bath and the temperature of the solution brought down to ambient. The reaction mixture was then poured over ice. The resultant aqueous mixture was adjusted to pH 9 with potassium carbonate and steam distilled. The aqueous distillate collected at 92°-96° C. was extracted with three portions of methylene chloride. The combined organic extract was dried over anhydrous sodium sulfate, filtered and distilled to afford 15.91 g (71% yield) of the title compound, b.p. 138°-140° C.; MS GC-MS M/Z: 146 (M+H)+ ; 1H NMR (CDCl3) d 2.53 (s, 3H), 7.23 (d, 1H, J=6.0 Hz), 8.37 (s, 1H).
後処理
- customequiped with a mechanical stirrer, a condenser
- temperaturethe reaction mixture was carefully heated to 35°-40° C
- customan exothermic reaction
- customto rise to 120° C.
- customThe flask was transferred to a cold water bath
- additionThe reaction mixture was then poured over ice
- distillationdistilled
- distillationThe aqueous distillate collected at 92°-96° C.
- extractionwas extracted with three portions of methylene chloride
- extractionThe combined organic extract
- dry with materialwas dried over anhydrous sodium sulfate
- filtrationfiltered
- distillationdistilled
出典と根拠
- ORDレコード
- ord-9c15659462ee47fb96bbf189ac58fe27
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05726182
関連ノート
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