Aklomide → 2-Chloro-4-nitrobenzonitrile

HRID 2295371

反応式

HRID 2295371 の反応式
S(Cl)(Cl)=O.[Cl:5][C:6]1[CH:14]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:7]=1[C:8]([NH2:10])=O>C1C=CC=CC=1>[Cl:5][C:6]1[CH:14]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:7]=1[C:8]#[N:10]

参加物

4

反応物 2

HCID 2075AklomideHCID 24386Thionyl Chloride

生成物 1

HCID 1414012-Chloro-4-nitrobenzonitrile収率 79.7%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

Thionyl chloride (1,000 g, 8.4 m) was then added to the 2-chloro-4-nitrobenzamide (200 g, 1 m) while the mixture was warmed. After addition, the mixture was refluxed for approximately three hours. The excess thionyl chloride was removed by distillation leaving a reaction mixture residue. Benzene (500 ml) was added to the cold reaction mixture residue to extract the reaction product. The extract was washed with diluted sodium hydroxide solution and water until neutralized and then dried over anhydrous sodium sulfate. The benzene solvent was distilled off and the reaction product was crystallized from methanol to yield 2-chloro-4-nitrobenzonitrile (145 g, 79%, mp 73°-75° C.).

後処理

  1. temperaturewas warmed
  2. additionAfter addition
  3. temperaturethe mixture was refluxed for approximately three hours
  4. customThe excess thionyl chloride was removed by distillation
  5. customleaving a reaction mixture residue
  6. extractionto extract the reaction product
  7. washThe extract was washed with diluted sodium hydroxide solution and water until neutralized and
  8. dry with materialthen dried over anhydrous sodium sulfate
  9. distillationThe benzene solvent was distilled off
  10. customthe reaction product was crystallized from methanol

出典と根拠

ORDレコード
ord-908ac15f209d4eec953a0050b68fc201
出典データセット
uspto-grants-1984_01
特許番号
US04424371

関連ノート

読み込み中…