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Acetone → 4-(2-Chloro-5-fluorophenyl)-3-buten-2-one

HRID 49196
ノート
印刷プレビュー

反応式

HRID 49196 の反応式
[OH-].[Na+].[Cl:3][C:4]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:5]=1[CH:6]=O.[CH3:13][C:14]([CH3:16])=[O:15]>O>[Cl:3][C:4]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][C:5]=1[CH:6]=[CH:13][C:14](=[O:15])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 180Acetone2 回HCID 14798Sodium HydroxideHCID 27791842-Chloro-5-Fluorobenzaldehyde

生成物 1

HCID 539229184-(2-Chloro-5-fluorophenyl)-3-buten-2-one

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Sodium hydroxide (0.78 g) was dissolved in water (55 ml) and treated dropwise with acetone (55 ml) followed by a solution of 2-chloro-5-fluorobenzaldehyde (2.8 g) in acetone (10 ml). The reaction mixture was stirred at room temperature for 2 hours. Acetone was distilled off under reduced pressure, and the residue was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and concentrated under reduced 5 pressure to obtain 4-(2-chloro-5-fluorophenyl)-3-buten-2-one (0.24 g).

後処理

  1. distillationAcetone was distilled off under reduced pressure
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe organic layer was washed successively with water and saturated brine
  4. concentrationconcentrated under reduced 5 pressure

出典と根拠

ORDレコード
ord-54bc9528b20642ac91a50a3cc2b0ba87
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06706732B1

反応ノート

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