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

HRID 1370182
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1370182
[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]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

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

Produkt 1

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

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

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%.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-64d2ea781a1a4ad992f99ad135a1190a
Quelldatensatz
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06583134B2

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