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Chloromethyl Methyl Ether → N-(methoxymethyl)-3-indolecarboxaldehyde

HRID 1985418
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HRID 1985418 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=[O:11])=[CH:2]1.[H-].[Na+].[CH3:14][O:15][CH2:16]Cl.[Cl-].[NH4+]>CN(C)C=O.O>[CH3:14][O:15][CH2:16][N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]=[O:11])=[CH:2]1
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참가 물질

7

반응물 4

HCID 7864Chloromethyl Methyl EtherHCID 10256Indole-3-CarboxaldehydeHCID 24758Sodium hydrideHCID 25517Ammonium Chloride

생성물 1

HCID 11137907N-(methoxymethyl)-3-indolecarboxaldehyde수율 20%

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

5 g of Indol-3-aldehyde was dissolved in 40 ml of N,N-dimethylformamide, and 1.38 g of 60% sodium hydride was added under ice-cooling. The reaction solution was stirred for 20 minutes with ice-cooling, then 3.2 ml of chloromethyl methyl ether was added, and stirring was continued at room temperature for 16 hours. The reaction solution was cooled in ice, treated with water and ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was subjected to silica gel column chromatography, to give 6.1 g of the title compound (20-44% ethyl acetate-hexane)

후처리

  1. temperaturecooling
  2. temperaturecooling
  3. stirringstirring
  4. waitwas continued at room temperature for 16 hours
  5. temperatureThe reaction solution was cooled in ice
  6. extractionextracted with ethyl acetate
  7. washThe organic layer was washed with saturated brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customevaporated

출처 및 근거

ORD 기록
ord-f5c1de5088d541d78e883ad691615c2e
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544835B2

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