3',5'-Difluoroacetophenone → 2-(3,5-Difluorophenyl)propan-2-ol

HRID 401787

反応式

HRID 401787 の反応式
[F:1][C:2]1[CH:3]=[C:4]([C:9](=[O:11])[CH3:10])[CH:5]=[C:6]([F:8])[CH:7]=1.[CH3:12][Mg]Br>C1COCC1>[F:1][C:2]1[CH:3]=[C:4]([C:9]([OH:11])([CH3:12])[CH3:10])[CH:5]=[C:6]([F:8])[CH:7]=1

参加物

4

反応物 2

HCID 5185963',5'-DifluoroacetophenoneHCID 178418573HCID 178418573、化合物

生成物 1

HCID 577321592-(3,5-Difluorophenyl)propan-2-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 1-(3,5-difluoro-phenyl)-ethanone (156 g, 1 mol, 1 eq) in THF (500 mL) was added dropwise under argon to the commercially available solution of methymagnesium bromide (143 g, 1.2 mol, 1.2 eq) in THF at such a rate that gentle refluxing was maintained. After the addition was complete the reaction mixture was stirred at ambient temperature for an hour and poured into ice-cold aqueous saturated ammonium chloride. Phases were separated and aqueous layer extracted two times with ethyl acetate. The combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. After removal of the solvent title compound was purified by distillation under reduced pressure (145 g, 0.84 mol, 84%).

後処理

  1. temperaturethat gentle refluxing
  2. temperaturewas maintained
  3. additionAfter the addition
  4. additionpoured into ice-cold aqueous saturated ammonium chloride
  5. customPhases were separated
  6. extractionaqueous layer extracted two times with ethyl acetate
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customAfter removal of the solvent title compound
  10. distillationwas purified by distillation under reduced pressure (145 g, 0.84 mol, 84%)

出典と根拠

ORDレコード
ord-a1eb185159174766a70ab795d9073411
出典データセット
uspto-grants-2014_06
特許番号
US08741934B2

関連ノート

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