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Nitric Acid → 2-Chloro-6-methyl-4-nitropyridin-N-oxide

HRID 333069
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HRID 333069 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N+:3]=1[O-:9].[N+:10]([O-])([OH:12])=[O:11]>S(=O)(=O)(O)O>[Cl:1][C:2]1[CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[CH:5]=[C:4]([CH3:8])[N+:3]=1[O-:9]
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참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 45797722-Chloro-6-methylpyridine 1-oxide

생성물 1

HCID 27518132-Chloro-6-methyl-4-nitropyridin-N-oxide수율 94%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

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온도
0 °C

실험 절차

2-Chloro-6-methyl-pyridine 1-oxide (5.0 g, 0.035 mol) was dissolved in concentrated sulfuric acid (20 ml) at 0° C. An ice-cooled mixture of concentrated nitric acid (12 ml) in concentrated sulfuric acid (20 ml) was added dropwise with stirring at 0° C. The cooling bath was removed, stirring was continued for 3 hours at 90° C. The mixture was poured into a mixture of icewater and ethyl acetate and the resulting precipitate was removed by filtration. The phases of the filtrate were separated, the aqueous phase was extracted several times with ethyl acetate, basified with NaOH and extracted again with ethyl acetate. The combined organic phases were dried over magnesium sulfate and the solvent removed under reduced pressure. The residue was combined with the filtered residue above to yield 6.21 g of a yellow solid (0.033 mol, 94%). MS (ESI) m/z=189.0 [M+1]+.

후처리

  1. additionwas added dropwise
  2. customThe cooling bath was removed
  3. stirringstirring
  4. additionThe mixture was poured into a mixture of icewater and ethyl acetate
  5. customthe resulting precipitate was removed by filtration
  6. customThe phases of the filtrate were separated
  7. extractionthe aqueous phase was extracted several times with ethyl acetate
  8. extractionextracted again with ethyl acetate
  9. dry with materialThe combined organic phases were dried over magnesium sulfate
  10. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-f32e00196d1942218866bd0bc895ac2b
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877934B2

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