Stannous Chloride → (3,4-Difluorophenyl)hydrazine

HRID 1241851ノート

反応式

HRID 1241851 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[F:9])[NH2:5].[N:10]([O-])=O.[Na+].[Sn](Cl)Cl>Cl.O>[F:1][C:2]1[CH:3]=[C:4]([NH:5][NH2:10])[CH:6]=[CH:7][C:8]=1[F:9]

参加物

6

反応条件

温度
-10 °C

実験手順

A stirred mixture of 3,4-difluoroaniline (12.9 g, 0.1 mol) in concentrated hydrochloric acid (60 mL) was chilled to −10° C. with an ice/methanol bath. A solution of sodium nitrite (6.9 g, 0.1 mol) in water (30 mL) was added at a rate which maintained the temperature of the reaction mixture below 10° C. After stirring for 2 hours, the reaction mixture was cooled to 0° C. and a solution of tin(II) chloride (56.88 g, 0.3 mol) in concentrated hydrochloric acid (50 mL) was added dropwise with vigorous stirring. Additional concentrated hydrochloric acid (150 mL) was added to the reaction mixture and stirring was continued for 2 hours. The reaction mixture was filtered to collect the precipitated hydrochloride salt of the title compound. This precipitate was dissolved in water (75 mL) and the resulting solution was basified with 50% aqueous sodium hydroxide and extracted with ethyl acetate. The organic extracts were dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo to provide the title intermediate as a brown oil (8.11 g, 57.4%).

後処理

  1. temperaturemaintained the temperature of the reaction mixture below 10° C
  2. temperaturethe reaction mixture was cooled to 0° C.
  3. stirringstirring
  4. waitwas continued for 2 hours
  5. filtrationThe reaction mixture was filtered
  6. customto collect the precipitated hydrochloride salt of the title compound
  7. dissolutionThis precipitate was dissolved in water (75 mL)
  8. extractionextracted with ethyl acetate
  9. dry with materialThe organic extracts were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-d7188a663c1347fe99f87ffb72011624
出典データセット
uspto-grants-2006_10
特許番号
US07115591B2

反応ノート

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