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Hydrochloric Acid → 3'-Chloro-5'-(pentafluorosulfur)acetophenone

HRID 1258527
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HRID 1258527 반응식
N[C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1.N([O-])=O.[Na+].[ClH:21]>[Cu]Cl>[Cl:21][C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 23668193Sodium NitriteHCID 581368521-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone

생성물 1

HCID 581374223'-Chloro-5'-(pentafluorosulfur)acetophenone

시약·촉매·용매 1

HCID 62652Cuprous chloride촉매

실험 절차

1-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone (150 mg, ex. 22a) was dissolved in semiconcentrated hydrochloric acid (6 ml). While stirring and cooling, sodium nitrite solution (40 mg dissolved in water) was added dropwise, in the course of which the temperature was not to exceed 5° C. On completion of formation of the diazonium salt, copper(I) chloride solution (68 mg dissolved in 2 ml of concentrated hydrochloric acid) was cooled to 0° C. while stirring and the above diazonium salt solution was slowly added dropwise. Then the cooling bath was removed, and the mixture was stirred at RT for 3 h and left to stand overnight. Then the reaction mixture was diluted with water and extracted repeatedly with EA. The combined EA phases were washed with saturated sodium hydrogencarbonate solution, dried over magnesium sulfate, filtered and concentrated. The residue was purified by means of preparative HPLC. The product-containing fractions were combined, freed of the acetonitrile, admixed with saturated sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined extracts were dried over magnesium sulfate, filtered and concentrated. 104 mg of the desired compound were obtained.

후처리

  1. temperaturecooling
  2. customto exceed 5° C
  3. stirringwhile stirring
  4. customThen the cooling bath was removed
  5. stirringthe mixture was stirred at RT for 3 h
  6. waitleft
  7. additionThen the reaction mixture was diluted with water
  8. extractionextracted repeatedly with EA
  9. washThe combined EA phases were washed with saturated sodium hydrogencarbonate solution
  10. dry with materialdried over magnesium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customThe residue was purified by means of preparative HPLC
  14. extractionextracted three times with ethyl acetate
  15. dry with materialThe combined extracts were dried over magnesium sulfate
  16. filtrationfiltered
  17. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6dcddc1150d1481b93d0e47a3e22b447
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08466169B2

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