Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 71743951 | HCID 71743951 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 86691622 | HCID 86691622 | 52% |
Reaction Steps
A mixture of 5-chloro-4-fluoro-2-(4-fluorophenyl)benzofuran-3-carbaldehyde (1.2 g, 4.10 mmol) and ethylenediamine (0.277 m, 4.10 mmol) in t-BuOH (15 ml) under a N2 atmosphere in a 50 ml RB flask was stirred at room temperature for 30 minutes. Potassium carbonate (0.567 g, 4.10 mmol) followed by iodine (1.041 g, 4.10 mmol) were then added and the reaction mixture was heated at 70° C. for 2 hours. The solvent was removed and the residue diluted with ethyl acetate. The mixture was washed with 10% sodium thiosulfate solution. The organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by using combiflash silica column using 8% methanol in chloroform as an eluent. The desired fractions were collected and concentrated to give the titled product (0.7 g, 52%). 1H NMR (400 MHz, CDCl3): δ 7.77-7.75 (m, 2H), 7.37-7.34 (m, 1H), 7.27-7.16 (m, 3H), 3.90 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09303020B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-69e2d26a34c647759db237b795bdc381 |
|---|
| Source note | uspto-grants-2016_04 |
|---|