Hydroxyamine hydrochloride → 2-Fluoro-3,4-dimethoxybenzonitrile

HRID 274492

反応式

HRID 274492 の反応式
[F:1][C:2]1[C:9]([O:10][CH3:11])=[C:8]([O:12][CH3:13])[CH:7]=[CH:6][C:3]=1[CH:4]=O.Cl.[NH2:15]O>C(O)C>[F:1][C:2]1[C:9]([O:10][CH3:11])=[C:8]([O:12][CH3:13])[CH:7]=[CH:6][C:3]=1[C:4]#[N:15]

参加物

4

反応物 2

HCID 443297Hydroxyamine hydrochlorideHCID 6035882-Fluoro-3,4-dimethoxybenzaldehyde

生成物 1

HCID 214590582-Fluoro-3,4-dimethoxybenzonitrile

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

4.4 g of 2-fluoro-3,4-dimethoxybenzaldehyde and 1.83 g of hydroxylamine hydrochloride are heated under reflux for 5 hours together with 30 ml of ethanol. The reaction mixture is subsequently evaporated and the residue, dried in a high vacuum at 23°, is introduced into 40 ml of phosphorus oxychloride. After stirring at 23° for 2.5 hours the reaction mixture is evaporated, the residue is treated with ice-water, the precipitate which thereby forms is filtered off, washed with water, taken up in methylene chloride, the methylene chloride solution is dried over sodium sulfate and evaporated. By recrystallization of the residue from methylene chloride/hexane there is obtained 2-fluoro-3,4-dimethoxybenzonitrile of m.p. 64°-65°.

後処理

  1. customThe reaction mixture is subsequently evaporated
  2. customthe residue, dried in a high vacuum at 23°
  3. additionis introduced into 40 ml of phosphorus oxychloride
  4. customis evaporated
  5. additionthe residue is treated with ice-water
  6. filtrationthe precipitate which thereby forms is filtered off
  7. washwashed with water
  8. dry with materialthe methylene chloride solution is dried over sodium sulfate
  9. customevaporated
  10. customBy recrystallization of the residue from methylene chloride/hexane there

出典と根拠

ORDレコード
ord-857d587f38c14afbb0770f841ce0efe5
出典データセット
uspto-grants-1995_02
特許番号
US05389653

関連ノート

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