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Ethyl Acetate → HCID 22277806, Verbindung

HRID 2055330
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2055330
[CH3:1][C:2]1[C:10]2[C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[S:7][C:6]=2[CH:5]=[CH:4][C:3]=1[N+:15]([O-])=O.CCOC(C)=O>C(O)C.[Pd]>[NH2:15][C:3]1[CH:4]=[CH:5][C:6]2[S:7][C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[C:10]=2[C:2]=1[CH3:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 8857Ethyl AcetateHCID 222777981-Methyl-2-nitrodibenzothiophene

Produkt 1

HCID 22277806HCID 22277806, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

1-Methyl-2-nitrodibenzothiophene (Method 11; 0.855 g, 3.52 mmol) was stirred in ethanol (50 ml) and EtOAc (50 ml) under an argon atmosphere. 10% Palladium on carbon (0.09 g) was added to the solution and the reaction mixture was stirred under a hydrogen atmosphere at room temperature for 3 h. The mixture was filtered through diatomaceous earth and washed with EtOAc before the filtrate was evaporated in vacuo. The crude product was purified by flash chromatography eluting with 50% DCM/iso-hexane-DCM. Evaporation of the appropriate fractions left the product as a colourless solid. NMR: 8.39 (m, 1H), 7.92 (m, 1H), 7.50 (m,1H), 7.42 (m, 2H), 6.92 (d, 1H), 4.98 (brs, 2H), 2.60 (s, 3H); m/z 215.

Aufarbeitung

  1. filtrationThe mixture was filtered through diatomaceous earth
  2. washwashed with EtOAc before the filtrate
  3. customwas evaporated in vacuo
  4. customThe crude product was purified by flash chromatography
  5. washeluting with 50% DCM/iso-hexane-DCM
  6. customEvaporation of the appropriate fractions
  7. waitleft the product as a colourless solid

Quellen und Nachweise

ORD-Eintrag
ord-f27db409cd4d46639a3c45ac006f22f6
Quelldatensatz
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07332492B2

Notizen zur Reaktion

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