HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-(1-Oxo-3-thienyl-2-propenyl)-2,2'-bithiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Acetyl-2,2'-bithienyl | HCID 606422 | — |
| Product | 5-(1-Oxo-3-thienyl-2-propenyl)-2,2'-bithiophene | HCID 67629095 | 84.1% |
Reaction Steps
1.1 g of 5-acetyl-2,2'-bithiophene was dissolved in 35 ml of ethanol, followed by adding 0.6 ml of 2-formyl-thiophene and KOH solution (KOH:H2O:ethanol=0.5 g:1 ml:5 ml). The color of the solution was turned into dark brown. Additional 0.1 ml of 2-formyl-thiophene was added to complete the reaction. The reaction solution was monitored by thin layer chromatography to determine whether the reaction was completed. The reaction mixture was kept in a refrigerator overnight. Decomposed with water and the crude product was collected. After the product was recrystallized from ethanol, 1.27 g of product was thus obtained and the melting point thereof was 135°-136° C. (yield: 84.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753692 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-4da0068a4ce0422ea886b32b657b7c0b |
| Source note | uspto-grants-1998_05 |