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Potassium Carbonate → 2-(3-Vinylphenylamino)-3-nitropyridine

HRID 1953405
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반응식

HRID 1953405 반응식
[CH:1]([C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6])=[CH2:2].Cl[C:11]1[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[CH:1]([C:3]1[CH:4]=[C:5]([NH:6][C:11]2[C:16]([N+:17]([O-:19])=[O:18])=[CH:15][CH:14]=[CH:13][N:12]=2)[CH:7]=[CH:8][CH:9]=1)=[CH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 796132-Chloro-3-nitropyridineHCID 42600413-Aminostyrene

생성물 1

HCID 232981282-(3-Vinylphenylamino)-3-nitropyridine수율 79.6%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A mixture of 3-vinylaniline (8 g), 2-chloro-3-nitropyridine (10.7 g) and potassium carbonate (18.6 g) in dioxane (80 ml) was stirred under reflux for 5 days. The reaction was extracted with chloroform, washed with water, dried over magnesium sulfate and evaporated. After evaporation of the solvent, crude residue was crystallized from methanol to give 2-(3-vinylphenylamino)-3-nitropyridine as an orange crystals (12.9 g).

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후처리

  1. temperatureunder reflux for 5 days
  2. extractionThe reaction was extracted with chloroform
  3. washwashed with water
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customAfter evaporation of the solvent, crude residue
  7. customwas crystallized from methanol

출처 및 근거

ORD 기록
ord-d16f2b570ac24227b348df00655d1766
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06117875

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