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Potassium Carbonate → 2-Chloro-6-methyl-4-nitropyridine

HRID 333070
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HRID 333070 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH3:11])[N+:3]=1[O-].P(Cl)(Cl)Cl.C(=O)([O-])[O-].[K+].[K+]>C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([CH3:11])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 24387Phosphorus trichlorideHCID 27518132-Chloro-6-methyl-4-nitropyridin-N-oxide

생성물 1

HCID 2986072-Chloro-6-methyl-4-nitropyridine

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2-Chloro-4-nitro-6-methyl-pyridine 1-oxide (6.2 g, 0.033 mol) was dissolved in chloroform (100 ml), phosphorus trichloride was added (22.6 g, 0.165 mol) and the mixture was heated under reflux for 2 days. The mixture was cooled to room temperature, poured into icewater and the mixture was neutralized with solid potassium carbonate. The phases were separated, the aqueous phase was extracted three times with chloroform, the combined organic phases were dried over magnesium sulfate. The solvent was removed under reduced pressure after which 5.326 g of a brown oil was obtained (0.031 mol, 94%) which was used directly in the next step.

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후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 days
  3. additionpoured into icewater
  4. customThe phases were separated
  5. extractionthe aqueous phase was extracted three times with chloroform
  6. dry with materialthe combined organic phases were dried over magnesium sulfate
  7. customThe solvent was removed under reduced pressure after which 5.326 g of a brown oil
  8. customwas obtained (0.031 mol, 94%) which

출처 및 근거

ORD 기록
ord-24932a00954f403ea0716094da62e798
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877934B2

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