2-Fluorobenzoyl chloride → 2,3-Dichloro-4-(2-fluorobenzoyl)phenetole

HRID 1154593ノート

反応式

HRID 1154593 の反応式
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[O:9][CH2:10][CH3:11].[F:12][C:13]1[CH:21]=[CH:20][CH:19]=[CH:18][C:14]=1[C:15](Cl)=[O:16].[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([C:15](=[O:16])[C:14]2[CH:18]=[CH:19][CH:20]=[CH:21][C:13]=2[F:12])[CH:5]=[CH:4][C:3]=1[O:9][CH2:10][CH3:11]

参加物

5

実験手順

A mixture of 2,3-dichlorophenetole (57.3 g., 0.3 mole), 2-fluorobenzoyl chloride (47.8 g., 0.3 mole) and methylene chloride (300 ml.) at 5° C. was stirred vigorously and treated with finely powdered aluminum chloride (42.6 g., 0.32 ml.). The reaction mixture was slowly warmed to room temperature and then stirred overnight. The reaction mixture was decomposed with ice/concentrated hydrochloric acid (50 ml.) and the aqueous solution was extracted twice with methylene chloride. The combined organic extracts were washed with aqueous sodium bicarbonate solution and finally with aqueous sodium chloride solution. The methylene chloride solution was dried over MgSO4 and filtered. The solvent was removed in vacuo and the residue on triturating with methanol gave the product 55 g., m.p. 94°-95° C. This material was used in the next step without additional purification.

後処理

  1. stirringstirred overnight
  2. extractionthe aqueous solution was extracted twice with methylene chloride
  3. washThe combined organic extracts were washed with aqueous sodium bicarbonate solution and finally with aqueous sodium chloride solution
  4. dry with materialThe methylene chloride solution was dried over MgSO4
  5. filtrationfiltered
  6. customThe solvent was removed in vacuo
  7. customthe residue on triturating with methanol

出典と根拠

ORDレコード
ord-6957526e7ec64774994257037395d6e5
出典データセット
uspto-grants-1984_12
特許番号
US04490384

反応ノート

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