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

HRID 1881356
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HRID 1881356 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 11430Potassium CarbonateHCID 36859272-Hydroxy-5-nitroindane

생성물 1

HCID 143168082-Methoxy-5-nitro-indan수율 74%

실험 절차

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).

후처리

  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)
  • 출처 및 근거

    ORD 기록
    ord-ec36f50090ef4a3cafe769c70aa25c45
    출처 데이터셋
    uspto-grants-2012_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08318790B2

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