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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-chloro-6-nitroquinoxaline → 2-Methoxy-6-nitroquinoxaline

HRID 1445474
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인쇄 미리보기

반응식

HRID 1445474 반응식
Cl[C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=2)[N:3]=1.[CH3:15][O-:16].[Na+]>C1COCC1>[CH3:15][O:16][C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-:14])=[O:13])[CH:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2357142-chloro-6-nitroquinoxalineHCID 10942334Sodium Methoxide

생성물 1

HCID 150258562-Methoxy-6-nitroquinoxaline수율 68.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Into 10 ml of THF was dissolved 1.16 g of 2-chloro-6-nitroquinoxaline, and then 1.0 g of sodium methoxide was added thereto, followed by heating under refluxing for 30 minutes. Then, the solvent was removed by evaporation. Water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline. After the solvent was removed by evaporation, the residue was crystallized from diethyl ether-hexane to obtain 776 mg of the title compound.

후처리

  1. temperatureby heating
  2. temperatureunder refluxing for 30 minutes
  3. customThen, the solvent was removed by evaporation
  4. additionWater was added to the residue
  5. extractionfollowed by extraction with ethyl acetate
  6. washThe organic layer was washed with saturated saline
  7. customAfter the solvent was removed by evaporation
  8. customthe residue was crystallized from diethyl ether-hexane

출처 및 근거

ORD 기록
ord-2c8ab18ae9184903844eccb33f4e62f3
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666873B2

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