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Water → HCID 13368505、化合物

HRID 1154507
ノート
印刷プレビュー

反応式

HRID 1154507 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8](=O)[N:7](C)[C:6]=2[CH:12]=1.O.[OH-].[K+]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([SH:9])=[C:6]([NH:7][CH3:8])[CH:12]=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 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 129578365-Chloro-3-methyl-1,3-benzothiazol-2(3H)-one

生成物 1

HCID 13368505HCID 13368505、化合物収率 98.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

5-Chloro-3-methyl-2-benzothiazolinone (70.0 g) was added to a mixture of water (118 ml), ethanol (350 ml) and potassium hydroxide (78.6 g). The solution was refluxed with stirring for three hours. After the solvent was evaporated under reduced pressure, the residual oil was dissolved in water. After removal of insoluble yellow crystals by filtration, the filtrate was neutralized with 2N-acetic acid, then resulting oily substance was extracted with ethyl acetate. The extract was washed with water, dried (Na2SO4), and evaporated to give oily 4-chloro-2-methylaminothiophenol (59.7 g). To a solution of sodium hydroxide (14.0 g) in water (100 ml) was added 4-chloro-2-methylaminothiophenol (59.6 g) with stirring, and then was added dropwise a solution of chloroacetic acid (34.0 g) in water (50 ml) at 20-25° C., followed by heating almost to boiling for three hours.

後処理

  1. temperatureThe solution was refluxed
  2. customAfter the solvent was evaporated under reduced pressure
  3. dissolutionthe residual oil was dissolved in water
  4. customAfter removal of insoluble yellow crystals
  5. filtrationby filtration
  6. extractionresulting oily substance was extracted with ethyl acetate
  7. washThe extract was washed with water
  8. dry with materialdried (Na2SO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-7c83e83a707c46f78b8873d6c7c336dd
出典データセット
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04490292

反応ノート

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