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Nitromethane → 7-[(E)-2-nitroethenyl]-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1-carbaldehyde

HRID 349569
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HRID 349569 반응식
[N:1]1([CH:11]=[O:12])[C:8]2[N:4]([N:5]=[CH:6][C:7]=2[CH:9]=O)[CH2:3][CH2:2]1.C([O-])(=O)C.[NH4+].[N+:18]([CH3:21])([O-:20])=[O:19]>>[N+:18](/[CH:21]=[CH:9]/[C:7]1[CH:6]=[N:5][N:4]2[CH2:3][CH2:2][N:1]([CH:11]=[O:12])[C:8]=12)([O-:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6375NitromethaneHCID 517165Ammonium AcetateHCID 179619742,3-dihydro-1H-imidazo[1,2-b]pyrazole-1,7-dicarbaldehyde

생성물 1

HCID 179619667-[(E)-2-nitroethenyl]-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1-carbaldehyde

실험 절차

A solution of 2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1,7-dicarbaldehyde (1 g) and ammonium acetate (653 mg) in nitromethane (20 ml) was refluxed for 4 hours. The reaction mixture was evaporated under reduced pressure and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give 7-[(E)-2-nitroethenyl]-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1-carbaldehyde (1.00 g).

후처리

  1. customThe reaction mixture was evaporated under reduced pressure
  2. extractionextracted with dichloromethane
  3. dry with materialThe extract was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9a07fa69d9b646a68acadc19aaa67ca9
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179801B2

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