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Potassium Iodide → 4-[Methyl(phenyl)amino]butan-1-ol

HRID 2248833
ノート
印刷プレビュー

反応式

HRID 2248833 の反応式
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:10][CH2:11][CH2:12][CH2:13][OH:14].[I-].[K+].C(=O)(O)[O-].[Na+]>CS(C)=O.O>[OH:14][CH2:13][CH2:12][CH2:11][CH2:10][N:2]([CH3:1])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 4875Potassium IodideHCID 7515N-MethylanilineHCID 1183884-BromobutanolHCID 516892Sodium Bicarbonate

生成物 1

HCID 100581054-[Methyl(phenyl)amino]butan-1-ol

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒
HCID 962
Water
溶媒

実験手順

A stirred solution of 107.2 g (1 mole) of N-methylaniline, 153.0 g (1 mole) of 4-bromo-1-butanol, 166 g (1 mole) of potassium iodide, and 168 g (2 mole) of sodium bicarbonate in dimethylsulfoxide is heated at 90° C. until the reaction is complete as indicated by thin layer chromatography. After cooling to room temperature, the reaction mixture is poured into a four-fold excess of water, and the aqueous solution is extracted with methylene chloride. The solvent is removed in vacuo, and the residual product is dissolved in a small amount of methylene chloride and swirled with silica gel. After removal of the silica gel, the solution is filtered through cotton and evaporated to yield compound A.

後処理

  1. extractionthe aqueous solution is extracted with methylene chloride
  2. customThe solvent is removed in vacuo
  3. dissolutionthe residual product is dissolved in a small amount of methylene chloride
  4. customAfter removal of the silica gel
  5. filtrationthe solution is filtered through cotton
  6. customevaporated

出典と根拠

ORDレコード
ord-293062daa9384489ac47621fe4ecf46a
出典データセット
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05041510

反応ノート

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