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Ethanol → 3-Fluoro-6-(phenylthio)-phenylacetic acid

HRID 435702
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HRID 435702 반응식
[F:1][C:2]1[CH:3]=[C:4](CC#N)[C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:7]=1.[CH2:18]([OH:20])[CH3:19].[OH-:21].[K+]>O>[F:1][C:2]1[CH:3]=[C:4]([CH2:19][C:18]([OH:21])=[O:20])[C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 12232352HCID 12232352, 화합물

생성물 1

HCID 122323553-Fluoro-6-(phenylthio)-phenylacetic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

80 g of 3-fluoro-6-(phenylthio)-phenylacetonitrile, 225 ml of ethanol, 75.5 g of potassium hydroxide and 225 ml of water are heated under reflux for 9 hours. The ethanol is subsequently evaporated off under reflux and the residue treated with water until completely dissolved, whereafter the neutral constituents are extracted with benzene. The aqueous solution is acidified with concentrated hydrochloric acid and extracted with chloroform. The organic phase is washed with water, dried over sodium sulphate and evaporated under reduced pressure. There is obtained 3-fluoro-6-(phenylthio)-phenylacetic acid which melts at 80°-83° C.

후처리

  1. temperatureunder reflux for 9 hours
  2. customThe ethanol is subsequently evaporated off
  3. temperatureunder reflux
  4. additionthe residue treated with water
  5. dissolutionuntil completely dissolved, whereafter the neutral constituents
  6. extractionare extracted with benzene
  7. extractionextracted with chloroform
  8. washThe organic phase is washed with water
  9. dry with materialdried over sodium sulphate
  10. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8051ab67dee0478abf4d9dd1648cb3a9
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04006144

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