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Ethanol → 4-((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)benzoic acid

HRID 747706
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인쇄 미리보기

반응식

HRID 747706 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:25]=[CH:24][CH:23]=[CH:22][C:16]=2C(OCC)=O)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-:26].[Na+].[CH2:28]([OH:30])C>>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([O:14][C:15]2[CH:16]=[CH:22][C:23]([C:28]([OH:30])=[O:26])=[CH:24][CH:25]=2)[CH2:12][CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 53995178Ethyl (1-t-butoxycarbonyl-4-piperidyloxy)benzoate

생성물 1

HCID 27946494-((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)benzoic acid

실험 절차

847 mg (2.43 mmol) of ethyl (1-t-butoxycarbonyl-4-piperidyloxy)benzoate was dissolved in 50 ml of ethanol. 5 ml of 1 N aqueous sodium hydroxide solution was added to the solution, and they were stirred at room temperature for 3 days. The reaction liquid was concentrated and then treated with ethyl acetate as the extractant in an ordinary manner to obtain the title compound.

후처리

  1. customThe reaction liquid
  • concentrationwas concentrated
  • additiontreated with ethyl acetate as the extractant in an ordinary manner
  • 출처 및 근거

    ORD 기록
    ord-6bb34d08400c4718b9b2b87d23b325e4
    출처 데이터셋
    uspto-grants-2008_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07396844B1

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