HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (2,4-Dichloro-phenyl)(6-iodo-benzofuran-2-yl)-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2',4'-Trichloroacetophenone | HCID 20250 | — |
| Reactant | 2-Hydroxy-4-iodobenzaldehyde | HCID 18351513 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2,4-Dichloro-phenyl)(6-iodo-benzofuran-2-yl)-methanone | HCID 59788945 | — |
Reaction Steps
To a solution of 4-iodo-2-hydroxy-benzaldehyde (5.4 g, 22 mmol) and 2-chloro-1-(2,4dichlorophenyl)ethanone (11.2 g, 50.0 mmol) in anhydrous N,N-dimethylformamide (100 mL) was added K2CO3 (12.0 g, 86.9 mmol). The dark brown reaction mixture was stirred at 90 C for 48 h, then poured onto water (150 mL) and extracted with ethyl acetate. The solvent was removed under reduced pressure and the residue was purified by column chromatography, eluting with 50% hexanes in dichloromethane. The desired product was obtained as an orange solid (2.06 g, 23%). 1H-NMR (CDCl3) δ 7.98 (s, 1H), 7.70 (dd, J=8.3, 1.3 Hz, 1H), 7.54-7.21 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420066B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2481382c178a47fdb1cac3a80d13ab25 |
| Source note | uspto-grants-2008_09 |