反応 #312574

ord-beed7d87c1d84a6db2065effe62dfba4

反応方程式

COc1ccccc1
Anisole
O=C(Cl)c1ccc(F)cc1
4-fluorobenzoyl chloride
Cl
HCl
[Al+3].[Cl-].[Cl-].[Cl-]
Aluminum chloride
COc1ccc(C(=O)c2ccc(F)cc2)cc1
4-fluoro-4′-methoxy-benzophenone
収率 94.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONpoured it
  2. 2
    その他separated
  3. 3
    抽出the aqueous layer was extracted with 2 portions of dichloromethane (300 mL each)
  4. 4
    洗浄washed with saturated aqueous sodium bicarbonate (400 mL)
  5. 5
    乾燥The organic layer was dried over anhydrous sodium sulfate
  6. 6
    その他evaporated

実験手順

Anisole (27.5 grams), 4-fluorobenzoyl chloride (35 grams) and dichloromethane (250 mL) were combined in a reaction flask. Aluminum chloride (30.8 grams) was added to the reaction mixture slowly over 20 minutes. Stirred the reaction mixture at room temperature for two hours and then poured it into a mixture of 70 mL concentrated HCl and 500 mL of water. The layers were phase separated and the aqueous layer was extracted with 2 portions of dichloromethane (300 mL each). The organic portions were combined and washed with saturated aqueous sodium bicarbonate (400 mL). The organic layer was dried over anhydrous sodium sulfate and evaporated to yielding 48.0 grams of 4-fluoro-4′-methoxy-benzophenone as a white solid. This material was not purified further but was used directly in the next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07556751B2uspto-grants-2009_07