ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetone → 2,6-Dichlorobenzylideneacetone

HRID 380938
ノート
印刷プレビュー

反応式

HRID 380938 の反応式
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:3]=1[CH:4]=O.[OH-].[Na+].O.C(OCC)(=O)C.[CH3:20][C:21]([CH3:23])=[O:22]>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:3]=1/[CH:4]=[CH:20]/[C:21](=[O:22])[CH3:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 180AcetoneHCID 962WaterHCID 67372,6-DichlorobenzaldehydeHCID 8857Ethyl AcetateHCID 14798Sodium Hydroxide

生成物 1

HCID 57087852,6-Dichlorobenzylideneacetone

実験手順

In a 250 ml single neck flask was charged 10 g (57 mmoles, 1.0 eq) of 2,6-dichlorobenzaldehyde dissolved in 100 ml of acetone. To this was added 2.28 g (5.7 mmoles, 0. 10eq.) of a 10% aqueous sodium hydroxide solution, dropwise and during the course of addition, temperature was kept no higher than 25°C., while the mixture was agitated continuously for 2 h. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to afford of (E)-4-(2,6-dichlorophenyl)-3-buten-2-one as a faintly yellow oil which was used directly in the following procedure.

後処理

  1. additiondropwise and during the course of addition, temperature
  2. customwas kept no higher than 25°C., while the mixture
  3. customthe phases were separated
  4. washthe organic phase was washed with water three times
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-ff298156f0d142a1bf130e1435b717a7
出典データセット
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06303818B1

反応ノート

読み込み中…

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