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Nitric Acid → 8-(4-Nitrophenyl)imidazo[1,2-a]pyridine

HRID 1982539
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HRID 1982539 반응식
[C:1]1([C:7]2[C:8]3[N:9]([CH:13]=[CH:14][N:15]=3)[CH:10]=[CH:11][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[N+:21]([O-])([OH:23])=[O:22].C(=O)([O-])[O-].[K+].[K+]>O>[N+:21]([C:4]1[CH:3]=[CH:2][C:1]([C:7]2[C:8]3[N:9]([CH:13]=[CH:14][N:15]=3)[CH:10]=[CH:11][CH:12]=2)=[CH:6][CH:5]=1)([O-:23])=[O:22]
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참가 물질

6

반응물 4

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 11430Potassium CarbonateHCID 137640278-Phenylimidazo[1,2-a]pyridine

생성물 1

HCID 233169598-(4-Nitrophenyl)imidazo[1,2-a]pyridine

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
-10 °C

실험 절차

Add 20 g (0.10 mole) of the product from Example 4 slowly to 150 ml of concentrated sulfuric acid at -15° C. Add 7 ml of concentrated nitric acid slowly, maintaining the temperature -10° C. Stir at -10° C. for 30 minutes. Pour onto 500 g of ice. Add 2 L of water and neutralize with potassium carbonate. Extract with three 500 ml portions of methylene chloride. Combine the extracts, dry over magnesium sulfate, treat with charcoal and remove the solvent in vacuo. The residue is crystallized from ether to provide the title compound.

후처리

  1. extractionExtract with three 500 ml portions of methylene chloride
  2. dry with materialdry over magnesium sulfate
  3. additiontreat with charcoal
  4. customremove the solvent in vacuo
  5. customThe residue is crystallized from ether

출처 및 근거

ORD 기록
ord-0ebf47bbc4ac40cca43b8ef2d7408410
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596872

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