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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl iodide → 3,8-Dimethoxy quinoline

HRID 399745
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HRID 399745 반응식
[OH:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13].[OH-].[K+].I[CH3:17]>C(O)C>[CH3:17][O:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 110843893-Quinolinol, 8-methoxy-2회

생성물 1

HCID 105837983,8-Dimethoxy quinoline수율 87.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

175 mg of 3-hydroxy-8-methoxy quinoline [compound (V)] prepared in example 6 and 66 mg of potassium hydroxide were added to 3 ml of ethanol, and the solution was agitated for 30 minutes. To the solution was added 284 mg of iodomethane, and the solution was agitated for 24 hours. The solvent was removed, and the solution was extracted with dichloromethane. The dichloromethane layer was washed with water and aqueous sodium hydroxide, and dried with anhydrous magnesium sulfate. The dichloromethane was removed by vacuum distillation to give 165 mg of 3,8-dimethoxy quinoline.

후처리

  1. stirringthe solution was agitated for 24 hours
  2. customThe solvent was removed
  3. extractionthe solution was extracted with dichloromethane
  4. washThe dichloromethane layer was washed with water and aqueous sodium hydroxide
  5. dry with materialdried with anhydrous magnesium sulfate
  6. customThe dichloromethane was removed by vacuum distillation

출처 및 근거

ORD 기록
ord-aaf958ebc6be4ebdac4f38df1b6371fc
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05824689

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