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Isoamyl Nitrite → 3-Fluoro-2-nitropyridine

HRID 626004
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HRID 626004 반응식
N[C:2]1[C:3]([N+:8]([O-:10])=[O:9])=[N:4][CH:5]=[CH:6][CH:7]=1.[F:11][B-](F)(F)F.[H+].N(OCCC(C)C)=O>C(O)C>[F:11][C:2]1[C:3]([N+:8]([O-:10])=[O:9])=[N:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8053Isoamyl NitriteHCID 28118Tetrafluoroboric acidHCID 832812-Nitropyridin-3-amine

생성물 1

HCID 27628023-Fluoro-2-nitropyridine수율 39%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

To a stirred solution of 3-Amino 2-nitro pyridine (2.5 g, 17.97 mmol) in dry ethanol (20 ml) was added 10 ml of tetrafluoroboric acid (48% in water). The reaction mixture was cooled to 0° C. and isoamyl nitrite (2.6 g, 22.4 mmol) was added dropwise at 0° C. and stirred at 0° C. for 1 hour. The reaction mixture was filtered, and the solid obtained was washed with diethyl ether. The filtered solid was added to preheated (150 mL) toluene with stirring and reaction mixture was refluxed for 24 hours. The solvent was evaporated and the residue taken in ethyl acetate (200 ml) and washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude 3-fluoro-2-nitropyridine. This was purified by column over silica gel using 10% ethyl acetate in pet ether as eluant to get 1 g (39%) of the title compound as a yellow solid.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customthe solid obtained
  3. washwas washed with diethyl ether
  4. additionThe filtered solid was added to preheated (150 mL) toluene
  5. stirringwith stirring
  6. customreaction mixture
  7. temperaturewas refluxed for 24 hours
  8. customThe solvent was evaporated
  9. washwashed with water
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated under reduced pressure
  12. customto get the crude 3-fluoro-2-nitropyridine
  13. customThis was purified by column over silica gel using 10% ethyl acetate in pet ether as eluant

출처 및 근거

ORD 기록
ord-37c62d4aa4704aa59012c2312f26e092
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309179B2

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