Reaktion #955964

ord-c065daf79bde4d3885c7e72645238f38

Reaktionsgleichung

CCCCCCCCC(CCCCCCCC)N1C(=O)c2c(Br)sc(Br)c2C1=O
1,3-Dibromo-5-(heptadecan-9-yl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione
CCO
ethanol
CC(=O)O
acetic acid
Cl
HCl
CCCCCCCCC(CCCCCCCC)N1C(=O)c2csc(Br)c2C1=O
1-bromo-5-(heptadecan-9-yl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturMixture was refluxed for one hour after which an aliquot
  2. 2
    Sonstigereaction
  3. 3
    TemperaturAfter cooling
  4. 4
    Filtrationthe solution was filtered through fritted glass
  5. 5
    Sonstigewas evaporated under vacuum
  6. 6
    SonstigeProduct was obtained by silica chromatography

Vorschrift

1,3-Dibromo-5-(heptadecan-9-yl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione (9.43 g, 20.04 mmol) and zinc (1.31 g, 20.04 mmol) were placed in a 3 neck round-bottom flask equipped with a water condenser with ethanol (130 mL), acetic acid (40 mL) and 1 M HCl (2.5 mL). Mixture was refluxed for one hour after which an aliquot was taken for NMR analysis, which indicated reaction was complete. After cooling, the solution was filtered through fritted glass to eliminate remaining Zn particles and solvent was evaporated under vacuum. Product was obtained by silica chromatography, using a 100% hexane to 100% CHCl3 gradient.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968885B2uspto-grants-2015_03