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Dichloromethane → (3-Hydroxy-6-methyl-pyridin-2-yl)-phenyl-methanone

HRID 228755
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HRID 228755 반응식
[OH:1][CH:2]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:3]1[C:8]([OH:9])=[CH:7][CH:6]=[C:5]([CH3:10])[N:4]=1.ClCCl>CO.[O-2].[O-2].[Mn+4]>[OH:9][C:8]1[C:3]([C:2]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[O:1])=[N:4][C:5]([CH3:10])=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 6344DichloromethaneHCID 230783712-(Hydroxyphenyl-methyl)-6-methyl-pyridin-3-ol

생성물 1

HCID 23078462(3-Hydroxy-6-methyl-pyridin-2-yl)-phenyl-methanone수율 80.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 887Methanol용매

실험 절차

2-(Hydroxy-phenyl-methyl)-6-methyl-pyridin-3-ol (553 mg) was dissolved in methanol (3 ml) and dichloromethane (9 ml) to prepare a solution. Manganese dioxide (2.05 g) was added to the solution, and the mixture was stirred at room temperature overnight. The reaction solution was filtered through Celite and was then washed with chloroform and methanol. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-acetone to give (3-hydroxy-6-methyl-pyridin-2-yl)-phenyl-methanone (439 mg, yield 80%).

후처리

  1. filtrationThe reaction solution was filtered through Celite
  2. washwas then washed with chloroform and methanol
  3. customThe solvent was removed by distillation under the reduced pressure
  4. customthe residue was purified by thin layer chromatography

출처 및 근거

ORD 기록
ord-c31a661dcc4d452bbf7cdfb82b918008
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560558B2

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