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Diethyl Ether → Ethyl (6-methoxy-1h-indol-3-yl)(oxo)acetate

HRID 54228
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인쇄 미리보기

반응식

HRID 54228 반응식
[C:1](Cl)(=[O:5])[C:2](Cl)=[O:3].[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[CH:14][NH:15]2)=[CH:11][CH:10]=1.[CH2:18]([O:20]CC)[CH3:19]>>[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([C:13]([C:1](=[O:5])[C:2]([O:20][CH2:18][CH3:19])=[O:3])=[CH:14][NH:15]2)=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 3283Diethyl EtherHCID 65578Oxalyl chlorideHCID 766596-Methoxy-1H-indole

생성물 1

HCID 19958885Ethyl (6-methoxy-1h-indol-3-yl)(oxo)acetate

실험 절차

7.5 cm3 of oxalyl chloride are added dropwise, under argon and over a period of 30 minutes, to a solution of 8.3 g of 6-methoxyindole, prepared in accordance with the process described by P. L. Feldman and H. Rapoport, Synthesis, (1986), 736, in 100 cm3 of anhydrous diethyl ether. After stirring for two hours, the precipitate formed is separated by filtration and then suspended in 200 cm3 of ethanol.

후처리

  1. customprepared in accordance with the process
  2. customRapoport, Synthesis, (1986), 736
  3. customthe precipitate formed
  4. customis separated by filtration

출처 및 근거

ORD 기록
ord-791a3c08f9704f98b7d1984cadf6dec0
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05622957

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