Hydrochloric Acid → 2,3-Dichloro-4-methoxy-4'-fluorobenzophenone

HRID 1439211

反応式

HRID 1439211 の反応式
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[O:9][CH3:10].[F:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](Cl)=[O:17])=[CH:14][CH:13]=1.[Cl-].[Al+3].[Cl-].[Cl-].Cl>C(Cl)Cl>[F:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([C:6]2[CH:5]=[CH:4][C:3]([O:9][CH3:10])=[C:2]([Cl:1])[C:7]=2[Cl:8])=[O:17])=[CH:14][CH:13]=1

参加物

6

実験手順

A mixture of 2,3-dichloroanisole (35.4 g.; 0.20 mole), 4-fluorobenzoyl chloride (34.8 g.; 0.22 mole) and methylene chloride (300 ml.) at 5° C. was stirred vigorously and treated with finely powdered aluminum chloride (28.0 g.; 0.21 mole). The reaction mixture was slowly heated and refluxed for two hours. The reaction mixture was cooled to room temperature and decomposed with ice and hydrochloric acid (50 ml.). The aqueous solution was extracted twice with methylene chloride. The combined methylene chloride solution was washed with aqueous sodium bicarbonate solution and finally with water. The organic layer was dried (MgSO4) and filtered. The solvent was removed in vacuo, and the residue on triturating with pet. ether gave the product 32 g. (50%); m.p. 138°-140°. This product was used for Step B without further purification.

後処理

  1. temperatureThe reaction mixture was slowly heated
  2. temperaturerefluxed for two hours
  3. extractionThe aqueous solution was extracted twice with methylene chloride
  4. washThe combined methylene chloride solution was washed with aqueous sodium bicarbonate solution and finally with water
  5. dry with materialThe organic layer was dried (MgSO4)
  6. filtrationfiltered
  7. customThe solvent was removed in vacuo
  8. customthe residue on triturating with pet. ether

出典と根拠

ORDレコード
ord-e544f0f0bcf4412dbc23835a0109dfb9
出典データセット
uspto-grants-1977_11
特許番号
US04058559

関連ノート

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