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

HRID 1700711
ノート
印刷プレビュー

反応式

HRID 1700711 の反応式
[OH-].[Na+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:12][CH3:13])=[C:8]([CH:11]=1)[CH:9]=O.[CH3:14][C:15]([CH3:17])=[O:16]>O>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:12][CH3:13])=[C:8]([CH:9]=[CH:14][C:15](=[O:16])[CH3:17])[CH:11]=1
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 37183565-Chloro-2-methoxybenzaldehyde

生成物 1

HCID 536609684-(5-Chloro-2-methoxyphenyl)-3-buten-2-one

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In water (100 ml) was dissolved sodium hydroxide (3.0 g), and to the solution was added acetone (80 ml) and then was added dropwise a solution of 5-chloro-2-methoxybenzaldehyde (11.8 g) in acetone (30 ml). The reaction solution was stirred at room temperature for 2 hours, and acetone was evaporated under reduced pressure. The residue was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine and concentrated under reduced pressure. The residue was purified with silica gel column chromatography to give 4-(5-chloro-2-methoxyphenyl)-3-buten-2-one (6.8 g).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customacetone was evaporated under reduced pressure
  2. extractionThe residue was extracted with ethyl acetate
  3. washthe organic layer was washed with water and saturated brine
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified with silica gel column chromatography

出典と根拠

ORDレコード
ord-ab7cdc2fdce54d36b9569af9c2294b54
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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