Acetic Acid → HCID 58261099, compound
Reaction equation
[Br:1][C:2]1[S:3][C:4](Br)=[C:5]2[C:9](=[O:10])[N:8]([CH:11]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[C:7](=[O:28])[C:6]=12.C(O)C.C(O)(=O)C.Cl>[Zn].C(Cl)(Cl)Cl.CCCCCC>[Br:1][C:2]1[S:3][CH:4]=[C:5]2[C:9](=[O:10])[N:8]([CH:11]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[C:7](=[O:28])[C:6]=12Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
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.
Workup
- temperatureMixture was refluxed for one hour after which an aliquot
- customreaction
- temperatureAfter cooling
- filtrationthe solution was filtered through fritted glass
- customwas evaporated under vacuum
- customProduct was obtained by silica chromatography
Sources & evidence
- ORD record
- ord-a5c0202711514cfcacaf2b5be9c4632c
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691931B2
Reaction notes
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