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Sulfuric Acid → HCID 15538329、化合物

HRID 844386
ノート
印刷プレビュー

反応式

HRID 844386 の反応式
[CH3:1][N:2]([CH3:10])[CH2:3][CH2:4][N:5]([CH3:9])[CH2:6][CH2:7][OH:8].[H-].[Na+].[C:13]([NH2:17])(=[O:16])[CH:14]=[CH2:15].S(=O)(=O)(O)O>>[CH3:1][N:2]([CH3:10])[CH2:3][CH2:4][N:5]([CH3:9])[CH2:6][CH2:7][O:8][CH2:15][CH2:14][C:13]([NH2:17])=[O: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 4

HCID 1118Sulfuric AcidHCID 6579Acrylamide2 回HCID 24758Sodium hydrideHCID 751712-((2-(Dimethylamino)ethyl)(methyl)amino)ethanol2 回

生成物 1

HCID 15538329HCID 15538329、化合物

実験手順

A 50 ml 3 neck round bottom flask was fitted with the following: magnetic stirrer, reflux condenser, air bubbler, and a temperature controlled oil bath. The flask was charged with 7.3 g of 2-{[2-(dimethylamino)ethyl]methylamino}ethanol. Sodium hydride, 0.014 g, was then added carefully to the of 2-{[2-(dimethylamino)ethyl]methylamino}ethanol with stirring. The mixture was stirred at a constant rate for two minutes before 3.55 g of acrylamide was added. After the addition of acrylamide, the reaction mixture was stirred at 50° C. for 6 hours. The mixture was cooled to ambient temperature. Concentrated sulfuric acid, 0.034 g, then was added to neutralize the product mixture. The resulting mixture was filtered through a Celite layer. The filtrate was collected for foam application. Quantitative 1H NMR showed that the product was 94% pure.

後処理

  1. temperaturereflux condenser
  2. additionwas added
  3. stirringthe reaction mixture was stirred at 50° C. for 6 hours
  4. filtrationThe resulting mixture was filtered through a Celite layer
  5. customThe filtrate was collected for foam application

出典と根拠

ORDレコード
ord-3f21d7c6b70e44728ce94e55f659199a
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380274B1

反応ノート

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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