Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 86717685 | HCID 86717685 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67293569 | HCID 67293569 | — |
Reaction Steps
To a 50 mL round bottom flask were added to 0.800 g of 2,5-bis(5,4 dibromo-3-tetradecyl-2-thienyl)-thiazolo[5,4-d]thiazole, 0.500 g Zn dust, 3 mL 3 M HCl, 2 mL acetic acid, 15 mL ethanol, and 15 mL toluene. The flask was heated to 100° C. for 3 hours. The reaction mixture was then filtered and the solvents were removed by rotary evaporation. The residue was purified by column chromatography using a mixture of hexane and dichloromethane to give the desired compound. The NMR data were obtained and were consistent with those of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09337358B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-cc57dee68c6747f2bfb742d4fbfb83ea |
|---|
| Source note | uspto-grants-2016_05 |
|---|