HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 1-[4-(2-Bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[3-(Tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanone | HCID 22929728 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[4-(2-Bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanone | HCID 22929670 | 69.8% |
Reaction Steps
Potassium carbonate (4.65 g, 33.7 mmol) and 1,2-dibromoethane (31.7 g, 166.6 mmol) were added to a solution of 1-[3-(tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanone (8.0 g, 33.7 mmol) in dimethylformamide (200 ml) and the mixture was stirred at room temperature for 12 hours. Ethyl acetate was added, the reaction mixture was washed with water and brine in that order and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield 1-[4-(2-bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanone (8.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244730B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-61e43feaafaa413aa50c4c690d6ee472 |
| Source note | uspto-grants-2007_07 |