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Hydrochloric Acid → HCID 178481857、化合物

HRID 1292807
ノート
印刷プレビュー

反応式

HRID 1292807 の反応式
[CH3:1][NH:2][NH2:3].Cl.[F:5][CH:6]([F:15])[C:7](=O)[CH2:8][C:9](OCC)=[O:10]>C(O)C>[F:5][CH:6]([F:15])[C:7]1[CH:8]=[C:9]([OH:10])[N:2]([CH3:1])[N:3]=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 6061MethylhydrazineHCID 67697Butanoic acid, 4,4-difluoro-3-oxo-, ethyl ester

生成物 1

HCID 178481857HCID 178481857、化合物収率 33.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

8.3 g (180.6 mmoles) of methylhydrazine and 5 ml of concentrated hydrochloric acid were added to a solution of 30.0 g (180.6 mmoles) of ethyl difluoroacetoacetate dissolved in 200 ml of ethanol. The mixture was refluxed for 2 days with heating, to give rise to a reaction. After the completion of the reaction, the reaction mixture was subjected to vacuum distillation to remove the most part of the solvent contained therein. The residue was poured into water. The mixture was allowed to have a pH of 4 using citric acid and extracted with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate mixed solvent) to obtain 8.9 g (yield: 33.3) of 3-difluoromethyl-1-methyl-1H-pyrazol-5-ol.

後処理

  1. temperatureThe mixture was refluxed for 2 days
  2. temperaturewith heating
  3. customto give rise
  4. customto a reaction
  5. customAfter the completion of the reaction
  6. distillationthe reaction mixture was subjected to vacuum distillation
  7. customto remove the most part of the solvent
  8. additionThe residue was poured into water
  9. extractionextracted with ethyl acetate
  10. washThe resulting organic layer was washed with water
  11. dry with materialan aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate
  12. distillationThe resulting solution was subjected to vacuum distillation
  13. customto remove the solvent
  14. customThe residue was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate mixed solvent)

出典と根拠

ORDレコード
ord-ff90e331f451457ca7e6e96788e4f924
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07238689B2

反応ノート

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