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Water → HCID 13368505, 화합물

HRID 1154507
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HRID 1154507 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 13368505HCID 13368505, 화합물수율 98.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-7c83e83a707c46f78b8873d6c7c336dd
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04490292

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