Acetic Acid → HCID 58261091, compound

HRID 868781Notes

Reaction equation

HRID 868781 reaction equation
[Br:1][C:2]1[S:3][C:4](Br)=[C:5]2[C:9](=[O:10])[N:8]([CH2:11][CH:12]([CH2:17][CH3:18])[CH2:13][CH2:14][CH2:15][CH3:16])[C:7](=[O:19])[C:6]=12.C(O)C.C(O)(=O)C.CCCCCC>Cl.[Zn].C(Cl)(Cl)Cl>[Br:1][C:2]1[S:3][CH:4]=[C:5]2[C:9](=[O:10])[N:8]([CH2:11][CH:12]([CH2:17][CH3:18])[CH2:13][CH2:14][CH2:15][CH3:16])[C:7](=[O:19])[C:6]=12

Participants

8

Procedure

1,3-Dibromo-5-(2-ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione (2.6 g, 5 mmol) was placed in a three neck round-bottom flask equipped with a water condenser with ethanol (35 mL), acetic acid (10 mL) and three drops of 1 M HCl. The mixture was heated until the starting material was fully dissolved. At this point, zinc (310 mg, 5 mmol) was added in one portion. Mixture was refluxed for one hour after which an aliquot was taken for GC analysis and NMR, indicating reaction completion. 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 (1.1 g, 52%), using a 100% hexane to 100% CHCl3 gradient.

Workup

  1. temperatureThe mixture was heated until the starting material
  2. dissolutionwas fully dissolved
  3. temperatureMixture was refluxed for one hour after which an aliquot
  4. customreaction completion
  5. temperatureAfter cooling
  6. filtrationthe solution was filtered through fritted glass
  7. customwas evaporated under vacuum
  8. customProduct was obtained by silica chromatography (1.1 g, 52%)

Sources & evidence

ORD record
ord-c82efb5a82bf49538180eebf7edde96c
Source dataset
uspto-grants-2015_03
Patent number
US08968885B2

Reaction notes

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