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

HRID 1985418
ノート
印刷プレビュー

反応式

HRID 1985418 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 11137907N-(methoxymethyl)-3-indolecarboxaldehyde収率 20%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228
Dimethylformamide
溶媒

実験手順

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)

後処理

  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

出典と根拠

ORDレコード
ord-f5c1de5088d541d78e883ad691615c2e
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07544835B2

反応ノート

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