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1-(4-Chloro-3-fluorophenyl)propan-2-one → 1-(4-Chloro-3-fluorophenyl)-2-methylpropan-2-ol

HRID 56305
ノート
印刷プレビュー

反応式

HRID 56305 の反応式
[CH3:1][Mg]Br.[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12](=[O:14])[CH3:13])=[CH:7][C:6]=1[F:15]>C1COCC1>[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([CH3:1])([OH:14])[CH3:13])=[CH:7][C:6]=1[F:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 110414731-(4-Chloro-3-fluorophenyl)propan-2-oneHCID 178418573HCID 178418573、化合物

生成物 1

HCID 900235431-(4-Chloro-3-fluorophenyl)-2-methylpropan-2-ol収率 88.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
76 °C

実験手順

To a solution of methylmagnesium bromide (100 mL, 100.0 mmol, 1.0 M in THF) was added a solution of 1-(4-chloro-3-fluorophenyl)propan-2-one (9.00 g, 48.20 mmol) in THF (20 mL) dropwise at 0° C. under N2 and the reaction mixture was heated at 76° C. for 12 h. It was then cooled to rt and quenched with saturated NH4Cl aqueous solution (50 mL) and the mixture was poured into water (200 mL). The resulting mixture was extracted with EtOAc (100 mL×4) and the combined organic phases were washed with brine (100 mL×2), dried over anhydrous Na2SO4 (50 g) and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=8:1) to give the title compound as yellow liquid (8.61 g, 88.2%).

後処理

  1. temperatureIt was then cooled to rt
  2. customquenched with saturated NH4Cl aqueous solution (50 mL)
  3. additionthe mixture was poured into water (200 mL)
  4. extractionThe resulting mixture was extracted with EtOAc (100 mL×4)
  5. washthe combined organic phases were washed with brine (100 mL×2)
  6. dry with materialdried over anhydrous Na2SO4 (50 g)
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=8:1)

出典と根拠

ORDレコード
ord-5493becf99cc4981bfea89b9537e77e2
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434695B2

反応ノート

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