Hydrochloric Acid → 1,3-Bis(4-fluorobenzoyl)benzene

HRID 1885660

反応式

HRID 1885660 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[C:5](Cl)(=[O:15])[C:6]1[CH:14]=[CH:13][CH:12]=[C:8]([C:9](Cl)=[O:10])[CH:7]=1.[F:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.Cl>>[F:17][C:18]1[CH:23]=[CH:22][C:21]([C:5]([C:6]2[CH:14]=[CH:13][CH:12]=[C:8]([C:9](=[O:10])[C:21]3[CH:22]=[CH:23][C:18]([F:17])=[CH:19][CH:20]=3)[CH:7]=2)=[O:15])=[CH:20][CH:19]=1

参加物

5

実験手順

Anhydrous aluminum chloride (160.0 g, 1.20 mol) was added to a stirred solution of isophthaloyl chloride (101.5 g, 0.50 mol) dissolved in fluorobenzene (480.5 g, 5.0 mol) over a five to ten minute period. The mixture was stirred at room temperature for one hour and then maintained at 70°-80° C. for four hours. After cooling, the reaction mixture was poured onto approximately 2000 g of ice containing 100 mL of concentrated hydrochloric acid. The resulting suspension was separated by decantation and washed several times with water. The organic layer was distilled to remove excess fluorobenzene and the solid residue was collected by filtration, washed with water, and dried at 100° C. The crude solid was recrystallized from approximately 1000 mL of toluene to afford 130.5 g (81% yield) of 1,3-bis(4-fluorobenzoyl)benzene; m.p. 177.5°-178.5° C.; 1H NMR (CDCl3) δ 6.8-8.3 (m, 12H, aromatic). Anal. Calcd. for C20H12F2O2 : C, 74.53%; H, 3.75%; F, 11.79%. Found: C, 74.33%; H, 3.59%; F, 11.42%.

後処理

  1. temperaturemaintained at 70°-80° C. for four hours
  2. temperatureAfter cooling
  3. customThe resulting suspension was separated by decantation
  4. washwashed several times with water
  5. distillationThe organic layer was distilled
  6. customto remove excess fluorobenzene
  7. filtrationthe solid residue was collected by filtration
  8. washwashed with water
  9. customdried at 100° C
  10. customThe crude solid was recrystallized from approximately 1000 mL of toluene

出典と根拠

ORDレコード
ord-bf9ed53aebce45c4bbc1fbd113e2f42e
出典データセット
uspto-grants-1992_09
特許番号
US05145942

関連ノート

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