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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → 4-(furan-2-ylmethoxy)-1H-indole-2-carboxylic acid

HRID 2267771
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인쇄 미리보기

반응식

HRID 2267771 반응식
C([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[C:12]([O:15][CH2:16][C:17]1[O:18][CH:19]=[CH:20][CH:21]=1)[CH:11]=[CH:10][CH:9]=2)=[O:5])C.[OH-].[K+].CCO>>[O:18]1[CH:19]=[CH:20][CH:21]=[C:17]1[CH2:16][O:15][C:12]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:13]=1[CH:14]=[C:6]([C:4]([OH:5])=[O:3])[NH:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 668419954-(furan-2-ylmethoxy)-1H-indole-2-carboxylic acid ethyl ester

생성물 1

HCID 668417594-(furan-2-ylmethoxy)-1H-indole-2-carboxylic acid

실험 절차

The 4-(furan-2-ylmethoxy)-1H-indole-2-carboxylic acid ethyl ester 94 obtained above is mixed with a 1M-solution of KOH in EtOH (13.3 ml, 13.3 mmol) and stirred for 24 hours. The solvent is then evaporated and the residue is partitioned between water and ether. The water layer is acidified with HCl and extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated to give a white powder.

후처리

  • customThe solvent is then evaporated
  • customthe residue is partitioned between water and ether
  • extractionextracted twice with EtOAc
  • washThe combined organic layers are washed with brine
  • dry with materialdried over anhydrous sodium sulfate
  • filtrationfiltered
  • customevaporated
  • customto give a white powder
  • 출처 및 근거

    ORD 기록
    ord-80f3d0ca9685452bb1732f97395471dc
    출처 데이터셋
    uspto-grants-2010_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07858781B2

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