Hydrochloric Acid → HCID 13423728、化合物

HRID 543377ノート

反応式

HRID 543377 の反応式
[CH:1]([C:3]1[CH:8]=[C:7]([C:9]([CH3:12])([CH3:11])[CH3:10])[CH:6]=[C:5]([S:13]([CH3:16])(=[O:15])=[O:14])[C:4]=1[OH:17])=[O:2].[Mn]([O-])(=O)(=O)=[O:19].[K+].Cl.[O-]S([O-])=O.[Na+].[Na+]>[OH-].[Na+]>[C:1]([C:3]1[CH:8]=[C:7]([C:9]([CH3:12])([CH3:11])[CH3:10])[CH:6]=[C:5]([S:13]([CH3:16])(=[O:15])=[O:14])[C:4]=1[OH:17])([OH:19])=[O:2]

参加物

6

実験手順

2.56 g (0.01 mol) of 2-formyl-4-(1,1-dimethylethyl)-6-methylsulfonylphenol are introduced into a solution of 1.58 g (0.01 mol) of potassium permanganate in 50 ml of 2N sodium hydroxide solution, and the mixture is heated on a steam bath for 30 minutes. The cooled solution is then adjusted to pH 2 with 2N hydrochloric acid and decolorized with concentrated Na2SO3 solution. The mixture is extracted three times with ethyl acetate, which is evaporated in vacuo and the residue is recrystallized from acetonitrile.

後処理

  1. temperaturethe mixture is heated on a steam bath for 30 minutes
  2. extractionThe mixture is extracted three times with ethyl acetate, which
  3. customis evaporated in vacuo
  4. customthe residue is recrystallized from acetonitrile

出典と根拠

ORDレコード
ord-aa59289f62e1400c8669ec0e0bec3574
出典データセット
uspto-grants-1987_04
特許番号
US04661636

反応ノート

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