Bromine → 3-Bromo-4-fluorobenzaldehyde

HRID 34602

反応式

HRID 34602 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[Cl-].[Cl-].[Cl-].[Al+3].[Br:14]Br>ClCCl>[Br:14][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:2]=1[F:1])[CH:6]=[O:7]

参加物

5

実験手順

A solution of 4-fluorobenzaldehyde (49.6 g) in dry dichloromethane (20 cm3) was added to a cooled (0° C.) suspension of powdered aluminium trichloride (90.4 g) in dry dichloromethane (100 cm3). Bromine (70.4 g) was added, and the mixture heated at the reflux temperature of 16 hours. After cooling, the reaction mixture was carefully poured onto ice and extracted with dichloromethane. The combined organic layers were washed with saturated sodium metabisulphite solution, water and brine, then dried over anhydrous magnesium sulphate. Evaporation of the solvent under reduced pressure gave a dark red oil, which was purified by distillation under reduced pressure, using a 4" Vigreux column to give 3-bromo-4-fluorobenzaldehyde (45.7 g) as an oil, boiling point 85°-108° C. at 8 mmHg.

後処理

  1. temperaturea cooled
  2. temperaturethe mixture heated at the reflux temperature of 16 hours
  3. temperatureAfter cooling
  4. additionthe reaction mixture was carefully poured onto ice
  5. extractionextracted with dichloromethane
  6. washThe combined organic layers were washed with saturated sodium metabisulphite solution, water and brine
  7. dry with materialdried over anhydrous magnesium sulphate
  8. customEvaporation of the solvent under reduced pressure
  9. customgave a dark red oil, which
  10. distillationwas purified by distillation under reduced pressure

出典と根拠

ORDレコード
ord-51f7bccd211f473794c0bb87181f8215
出典データセット
uspto-grants-1988_08
特許番号
US04762835

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