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Nitroethane → 8-(2-Nitro-propenyl)-2,3-dihydro-1H-3a,6-diaza-cyclopenta[a]indene

HRID 1370182
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HRID 1370182 반응식
[CH2:1]1[C:5]2=[C:6]([CH:13]=O)[C:7]3[CH:8]=[N:9][CH:10]=[CH:11][C:12]=3[N:4]2[CH2:3][CH2:2]1.C([O-])(=O)C.[NH4+].[N+:20]([CH2:23][CH3:24])([O-:22])=[O:21]>>[N+:20]([C:23]([CH3:24])=[CH:13][C:6]1[C:7]2[CH:8]=[N:9][CH:10]=[CH:11][C:12]=2[N:4]2[CH2:3][CH2:2][CH2:1][C:5]=12)([O-:22])=[O:21]
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4

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HCID 6587NitroethaneHCID 517165Ammonium AcetateHCID 155163562,3-Dihydro-1H-3a,6-diaza-cyclopenta[a]indene-8-carbaldehyde

생성물 1

HCID 696404338-(2-Nitro-propenyl)-2,3-dihydro-1H-3a,6-diaza-cyclopenta[a]indene수율 77%

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온도
100 °C

실험 절차

To a solution of 2,3-dihydro-1H-3a,6-diaza-cyclopenta[a]indene-8-carbaldehyde (0.30 g 1.6 mMol) in nitroethane (3.00 ml) was added ammonium acetate (0.30 g 3.9 mMol) and the mixture was heated to 100° C. for 4 h with stirring under argon. The mixture was cooled to room temperature and purified by chromatography on silicagel gel (ca 30 g) eluting first with ethyl acetate (ca 100 ml) then with a mixture of ethyl acetate (9 parts) and methanol (1 part). The product fraction were combined, concentrated and the residue was recrystallised from ethyl acetate to yield the title compound (0.30 g, 77%) as yellow crystals. mp 141-142° C. Found C, 64.05; H, 5.51; N, 17.14%; C13H13N3O2 requires C, 64.19; H, 5.39; N, 17.27%.

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. custompurified by chromatography on silicagel gel (ca 30 g)
  3. washeluting first with ethyl acetate (ca 100 ml)
  4. additionwith a mixture of ethyl acetate (9 parts) and methanol (1 part)
  5. concentrationconcentrated
  6. customthe residue was recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-64d2ea781a1a4ad992f99ad135a1190a
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06583134B2

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