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Methanol → 2-Chloro-3,6-dimethoxyquinoxaline

HRID 464266
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HRID 464266 반응식
[Na].[Cl:2][C:3]1[C:12](Cl)=[N:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:14][CH3:15])[CH:9]=2)[N:4]=1.[CH3:16][OH:17]>>[Cl:2][C:3]1[C:12]([O:17][CH3:16])=[N:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:14][CH3:15])[CH:9]=2)[N:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887Methanol2회HCID 6842272,3-Dichloro-6-methoxyquinoxalineHCID 5360545Sodium

생성물 1

HCID 133856742-Chloro-3,6-dimethoxyquinoxaline

반응 조건

온도
50 °C

실험 절차

In a flame-dri ed reaction flask under a dry nitrogen atmosphere, there was slowly added a solution consisting of 850 mg. of sodium dissolved in 80 ml. of methanol to a slurry of 7.1 g. of 2,3-dichloro-6-methoxyquinoxaline in 60 ml. of methanol at 50° C. over a period of seven hours. The resulting mixture was then heated at 50° C. overnight and finally cooled to room temperature. Upon completion of this step, the spent reaction mixture was concentrated in vacuo and the residue subsequently dissolved in chloroform, followed by washing with water and drying over anhydrous magnesium sulfate. After removal of the drying agent by means of filtration and the solvent by means of evaporation under reduced pressure, the resulting resiuue was subsequently chromatographed on a column of 400 ml. of silica gel, followed by elution with toluene. The good fractions were combined and concentrated in vacuo to ultimately afford a white solid consisting of 6.1 g (88%) of pure 2-chloro-3,6-methoxyquinoxaline m.p. 79°-81° C.

후처리

  1. customreaction flask under a dry nitrogen atmosphere
  2. additionthere was slowly added a solution
  3. temperaturefinally cooled to room temperature
  4. customUpon completion of this step, the spent reaction mixture
  5. concentrationwas concentrated in vacuo
  6. dissolutionthe residue subsequently dissolved in chloroform
  7. washby washing with water
  8. dry with materialdrying over anhydrous magnesium sulfate
  9. customAfter removal of the drying agent
  10. filtrationby means of filtration
  11. customthe solvent by means of evaporation under reduced pressure
  12. customthe resulting resiuue was subsequently chromatographed on a column of 400 ml
  13. washof silica gel, followed by elution with toluene
  14. concentrationconcentrated in vacuo
  15. customto ultimately afford a white solid

출처 및 근거

ORD 기록
ord-5d521319636b4097a309727c6e2aed75
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04547501

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