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4-Chlorobenzaldehyde → HCID 53722686、化合物

HRID 1599795
ノート
印刷プレビュー

反応式

HRID 1599795 の反応式
[OH-].[K+].[CH:3]([CH:6]1[CH2:10][CH2:9][CH2:8][C:7]1=[O:11])([CH3:5])[CH3:4].[Cl:12][C:13]1[CH:20]=[CH:19][C:16]([CH:17]=O)=[CH:15][CH:14]=1>O>[CH:3]([CH:6]1[CH2:10][CH2:9][C:8](=[CH:17][C:16]2[CH:19]=[CH:20][C:13]([Cl:12])=[CH:14][CH:15]=2)[C:7]1=[O:11])([CH3:5])[CH3:4]
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

5

反応物 3

HCID 77264-ChlorobenzaldehydeHCID 14797Potassium HydroxideHCID 111709762-Isopropylcyclopentanone

生成物 1

HCID 53722686HCID 53722686、化合物収率 98.7%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
120 °C

実験手順

A solution of 1.1 g of 85% strength aqueous potassium hydroxide solution and 100 ml of water was charged to a 0.31 stainless-steel autoclave, and then 25.2 g of 2-isopropylcyclopentanone and 28.1 g of 4-chlorobenzaldehyde were added, and the mixture was heated to 120° C. under the intrinsic pressure and subsequently stirred at this temperature (intrinsic pressure 1 bar) for 5 hours. After cooling to room temperature, the suspension was filtered with suction and the product was washed to neutrality with water and then dried in a vacuum oven at 55° C. In this way 46.8 g of 2-isopropyl-5-(4-chlorobenzylidene)-cyclopentanone (98.7% pure) were obtained. This corresponds to a yield of 93% of theory.

後処理

  1. temperatureAfter cooling to room temperature
  2. filtrationthe suspension was filtered with suction
  3. washthe product was washed
  4. customdried in a vacuum oven at 55° C

出典と根拠

ORDレコード
ord-95a42d949e5a43019c2ce2b272a026ae
出典データセット
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05741937

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート