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

HRID 1258527
ノート
印刷プレビュー

反応式

HRID 1258527 の反応式
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
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 313Hydrochloric AcidHCID 23668193Sodium NitriteHCID 581368521-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone

生成物 1

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

試薬・触媒・溶媒 1

HCID 62652Cuprous chloride触媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-6dcddc1150d1481b93d0e47a3e22b447
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08466169B2

反応ノート

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