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Nitromethane → HCID 68553487, 화합물

HRID 2381275
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HRID 2381275 반응식
[CH3:1][O:2][C:3]1[C:11](OC)=[CH:10][CH:9]=[C:8]2[C:4]=1[C:5]([CH:14]=O)=[CH:6][NH:7]2.[C:16]([O-:19])(=O)C.[NH4+].[N+:21]([CH3:24])([O-:23])=[O:22]>>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[C:5]([CH:14]=[CH:24][N+:21]([O-:23])=[O:22])=[C:6]([O:19][CH3:16])[NH:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6375NitromethaneHCID 517165Ammonium AcetateHCID 111484124,5-dimethoxy-1H-indole-3-carbaldehyde

생성물 1

HCID 68553487HCID 68553487, 화합물수율 99%

실험 절차

A solution of 4,5-dimethoxyindole-3-carbaldehyde (0.21 g, 1.02 mmol) and ammonium acetate (0.1268 g, 1.60 mmol) in nitromethane (10 cm3) was stirred at 70-75° C. under nitrogen for 11 hours using the method of Macor et al. The mixture was concentrated under vacuum and partitioned between water and ethyl acetate. The organic layer was washed with brine, dried with MgS04, and evaporated under vacuum to afford dimethoxy-3-(2-nitroethenyl)indole (0.25 g, 99%) as a brown solid.

후처리

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
was concentrated under vacuum
  • custompartitioned between water and ethyl acetate
  • washThe organic layer was washed with brine
  • customdried with MgS04
  • customevaporated under vacuum
  • 출처 및 근거

    ORD 기록
    ord-7bb9da443a7a4a399cf5eeb0a64b80dd
    출처 데이터셋
    uspto-grants-2012_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08258173B2

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