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Hydrazine → 2,3,5,6-Tetrafluoro-4-hydrazinopyridine

HRID 1391434
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HRID 1391434 반응식
[F:1][C:2]1[N:7]=[C:6]([F:8])[C:5]([F:9])=[C:4](F)[C:3]=1[F:11].[NH2:12][NH2:13]>ClCCl>[F:1][C:2]1[C:3]([F:11])=[C:4]([NH:12][NH2:13])[C:5]([F:9])=[C:6]([F:8])[N:7]=1
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참가 물질

4

반응물 2

HCID 9321HydrazineHCID 69690Pentafluoropyridine

생성물 1

HCID 20640312,3,5,6-Tetrafluoro-4-hydrazinopyridine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Pentafluoropyridine (3.4 g; 20 mmol) was dissolved in dichloromethane (50 mL) and chilled in an ice bath. To the solution was added hydrazine (640 mg; 22 mmol) and it was stirred overnight. The solvent was evaporated, and the residue was dissolved in dichloromethane (50 mL) and washed with a 10% sodium carbonate solution (5 mL). It was dried over magnesium sulfate, and evaporated, to give crude 2,3,5,6-tetrafluoro-pyridin-4-yl-hydrazine. The crude product was then dissolved in ethanol. To the solution was added one drop of acetic acid, and m-tolylaldehyde (1.45 g; 12 mmol) and it was heated at 60° C. overnight. The resulting precipitate was filtered and dried to give N-(3-methyl-benzylidene)-N′-(2,3,5,6-tetrafluoro-pyridin-4-yl)-hydrazine (2.2 g).

후처리

  1. temperaturechilled in an ice bath
  2. customThe solvent was evaporated
  3. dissolutionthe residue was dissolved in dichloromethane (50 mL)
  4. washwashed with a 10% sodium carbonate solution (5 mL)
  5. dry with materialIt was dried over magnesium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-5c4561db0649427ea570b5d226eaa046
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07338951B2

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