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

HRID 1700719
ノート
印刷プレビュー

反応式

HRID 1700719 の反応式
[OH-].[Na+].O.[Cl:4][C:5]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][C:6]=1[CH:7]=O.[CH3:14][C:15]([CH3:17])=[O:16]>>[Cl:4][C:5]1[CH:12]=[CH:11][C:10]([CH3:13])=[CH:9][C:6]=1[CH:7]=[CH:14][C:15](=[O:16])[CH3:17]
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 4

HCID 180Acetone2 回HCID 962WaterHCID 14798Sodium HydroxideHCID 156472782-Chloro-5-methylbenzaldehyde

生成物 1

HCID 541354784-(2-Chloro-5-methylphenyl)-3-buten-2-one

実験手順

To a mixture of acetone (160 ml), sodium hydroxide (2.6 g) and water (160 ml) was added dropwise at 0° C. a solution of crude 2-chloro-5-methylbenzaldehyde (18.3 g) in acetone (30 ml), and the mixture was stirred at the same temperature for 1 hour. Under reduced pressure, acetone was evaporated, and the residue was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and concentrated under reduced pressure to give 4-(2-chloro-5-methylphenyl)-3-buten-2-one (18.9 g) as oil.

後処理

  1. customUnder reduced pressure, acetone was evaporated
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated brine
  4. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-109ff9bfa5c14315b7ec696f64e3584d
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350749B1

反応ノート

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