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

HRID 1370182
ノート
印刷プレビュー

反応式

HRID 1370182 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

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

生成物 1

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

反応条件

温度
100 °C

実験手順

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%.

後処理

  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

出典と根拠

ORDレコード
ord-64d2ea781a1a4ad992f99ad135a1190a
出典データセット
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06583134B2

反応ノート

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