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Potassium Carbonate → 2-Methoxy-5-nitro-indan

HRID 1422850
ノート
印刷プレビュー

反応式

HRID 1422850 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([OH:13])[CH2:7]2)([O-:3])=[O:2].[C:14]([O-])([O-])=O.[K+].[K+]>>[CH3:14][O:13][CH:8]1[CH2:7][C:6]2[C:10](=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[CH2:9]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 11430Potassium CarbonateHCID 36859272-Hydroxy-5-nitroindane

生成物 1

HCID 143168082-Methoxy-5-nitro-indan収率 74%

実験手順

5-nitro-indan-2-ol (1.55 g, 8.65 mmol) and K2CO3 (2.8 g, 20 mmol) was charged into a schlenk flask. The flask was evacuated and back filled with N2. DMF (10 mL) was added and stirred at r.t. for 30 min. MeI (excess, 10 mL) was added and the reaction mixture was stirred at 100° C. overnight. The reaction mixture was allowed to cool to room temperature. Water was added and the reaction mixture was extracted with EtOAc. The combined organic layers were washed with water and brine and dried over Na2SO4. Purification of the concentrated crude product by column chromatography (EtOAc:Hexane=1:9) afforded the title product as a pale yellow oil (520 mg, 74% based on recovered starting material).

後処理

  1. customThe flask was evacuated
  2. additionback filled with N2
  • additionDMF (10 mL) was added
  • additionMeI (excess, 10 mL) was added
  • stirringthe reaction mixture was stirred at 100° C. overnight
  • temperatureto cool to room temperature
  • additionWater was added
  • extractionthe reaction mixture was extracted with EtOAc
  • washThe combined organic layers were washed with water and brine
  • dry with materialdried over Na2SO4
  • customPurification of the
  • concentrationconcentrated crude product by column chromatography (EtOAc:Hexane=1:9)
  • 出典と根拠

    ORDレコード
    ord-b3bf7b0e633a438985e6582481474211
    出典データセット
    uspto-grants-2015_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08927548B2

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