HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Bromo-3-ethoxy-2,2',4'-trifluorobiphenyl-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-2,2',4'-trifluoro-3-hydroxybiphenyl-4-carbaldehyde | HCID 117992239 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-3-ethoxy-2,2',4'-trifluorobiphenyl-4-carbaldehyde | HCID 118037985 | 90.5% |
Reaction Steps
Iodoethane (0.77 g) was added at room temperature to a mixture of 6-bromo-2,2′,4′-trifluoro-3-hydroxybiphenyl-4-carbaldehyde (1.09 g), potassium carbonate (0.91 g), and DMF (20 mL), and the mixture was stirred at 60 C for 2 hours in a nitrogen atmosphere. Water was added to the reaction mixture at room temperature, followed by extraction with ethyl acetate. The organic layer was separated, washed with water and saturated saline in this order, and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (1.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120777B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0ec9e0c92d6948758fe3f4973fd19086 |
| Source note | uspto-grants-2015_09 |