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Diethyl Ether → 1-methyl-3-(4-methylphenyl)-1H-indole

HRID 1868539
ノート
印刷プレビュー

反応式

HRID 1868539 の反応式
Br[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]([CH3:11])[CH:3]=1.CCO[CH2:15][CH3:16].[NH4+].[Cl-]>>[CH3:11][N:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:2]([C:5]2[CH:10]=[CH:9][C:15]([CH3:16])=[CH:7][CH:6]=2)=[CH:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 3283Diethyl EtherHCID 25517Ammonium ChlorideHCID 133577363-Bromo-1-methyl-1H-indole

生成物 1

HCID 589315421-methyl-3-(4-methylphenyl)-1H-indole

実験手順

A mixture of 4.31 g (0.02 mol) of 3-bromo-1-methyl-1H-indole and 0.22 g (0.0004 mol) of NiCl2dppp was added to a solution of p-TolylMgBr in ether (prepared from 0.6 g of Mg (0.025 mol) and 4.21 g of TolylBr (0.024 mol) in 40 mL of ether) under stirring. The reaction mixture was stirred overnight. The resulting mixture was treated with 10% aqueous NH4Cl, the organic layer was separated, washed with 10% aqueous NH4Cl and then dried over anhydrous Na2SO4. The solution was evaporated to give an oil that crystallized. The product was washed with methanol and dried. Yield 2.2 g (49%) of colorless crystalline solid.

後処理

  • stirringThe reaction mixture was stirred overnight
  • customthe organic layer was separated
  • washwashed with 10% aqueous NH4Cl
  • dry with materialdried over anhydrous Na2SO4
  • customThe solution was evaporated
  • customto give an oil
  • customthat crystallized
  • washThe product was washed with methanol
  • customdried
  • 出典と根拠

    ORDレコード
    ord-217f396e4bd643be86f89975759c2c32
    出典データセット
    uspto-grants-2009_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07635781B2

    反応ノート

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