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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl chloroacetate → (1H-Indol-6-yloxy)-acetic acid methyl ester

HRID 399017
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반응식

HRID 399017 반응식
[OH:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.Cl[CH2:12][C:13]([O:15][CH3:16])=[O:14].C(=O)([O-])[O-].[K+].[K+]>[I-].[K+].CC(C)=O>[CH3:16][O:15][C:13]([CH2:12][O:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1)=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7295Methyl chloroacetateHCID 11430Potassium CarbonateHCID 5245086-Hydroxyindole

생성물 1

HCID 18969559(1H-Indol-6-yloxy)-acetic acid methyl ester수율 63.3%

시약·촉매·용매 2

HCID 4875Potassium Iodide촉매HCID 180Acetone용매

실험 절차

6-Hydroxyindole (2.9 g), methyl chloroacetate (2.7 g), potassium carbonate (5.5 g) and potassium iodide (0.2 g) are added to acetone (100 ml), and the mixture is refluxed for 8 hours. The reaction mixture is cooled to room temperature, and the insoluble materials are removed by filtration. The filtrate is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent; chloroform) to give 6-methoxycarbonylmethoxyindole (2.83 g).

후처리

  1. temperaturethe mixture is refluxed for 8 hours
  2. customthe insoluble materials are removed by filtration
  3. customThe filtrate is evaporated under reduced pressure
  4. customThe residue is purified by silica gel column chromatography (eluent; chloroform)

출처 및 근거

ORD 기록
ord-59f19f98a90542538f9d78d9b52ab590
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05817689

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