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Potassium Hydroxide → 2-(4-Methoxy-3-nitrophenylamino)ethanol

HRID 751544
ノート
印刷プレビュー

反応式

HRID 751544 の反応式
[OH-].[K+].[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:15][CH2:14][O:13]C2=O)=[CH:7][C:6]=1[N+:17]([O-:19])=[O:18]>CO.O>[OH:13][CH2:14][CH2:15][NH:11][C:8]1[CH:9]=[CH:10][C:5]([O:4][CH3:3])=[C:6]([N+:17]([O-:19])=[O:18])[CH:7]=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 2

HCID 14797Potassium HydroxideHCID 25110856HCID 25110856、化合物

生成物 1

HCID 144537412-(4-Methoxy-3-nitrophenylamino)ethanol

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

Solid potassium hydroxide (3.5 g) is dissolved in methanol (100 ml). To the obtained solution the 3-(4-methoxy-3-nitrophenyl)-1,3-oxazolidin-2-one of step 1.1 (5 g) is added whereupon a yellow suspension is formed. Then the reaction mixture is heated under reflux for 5 hours and a red solution is obtained. With stirring, diluted acetc acid (3.7 g in 20 ml water) is added dropwise to the warm solution and the reaction mixture is cooled down to from about 0° C. to about 5° C. An orange suspension is obtained, which is filtered. The resulting solid is dried.

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. customis formed
  2. temperatureThen the reaction mixture is heated
  3. temperatureunder reflux for 5 hours
  4. customa red solution is obtained
  5. additionis added dropwise to the warm solution
  6. temperaturethe reaction mixture is cooled down to from about 0° C. to about 5° C
  7. customAn orange suspension is obtained
  8. filtrationwhich is filtered
  9. customThe resulting solid is dried

出典と根拠

ORDレコード
ord-921f4043ed644bae89bd5c61a19d4735
出典データセット
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07405325B2

反応ノート

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