HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 66626477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | [2,2'-Bithiophene]-5-carboxaldehyde | HCID 364428 | — |
| Reactant | HCID 86616915 | HCID 86616915 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66626477 | HCID 66626477 | — |
Reaction Steps
One-step synthesis of the title compound can be achieved by combining 2,5-diaminothiophene-3,4-dicarboxylate (15 mg, 0.5 mmol) with 2-thiophene carboxaldehyde (6.5 mg, 0.6 mmol), followed by refluxing in ethanol for 12 hours in the presence of a catalytic amount of TFA. After removal of the solvent, 5-(thiophen-2-yl)thiophene-2-carbaldehyde (11.3 mg, 0.5 mmol) in isopropanol was added in addition to a catalytic amount of TFA and the solution refluxed for 12 hours. The title compound was isolated as a red powder (20.9 mg, 0.4 mmol, 63%) after flash chromatography (SiO2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034895B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-6bd7f2fe446f4937b486b02b4be6fcb2 |
| Source note | uspto-grants-2011_10 |