HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 1-(4-Bromo-2-nitrophenyl)butane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoate | HCID 86694315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Bromo-2-nitrophenyl)butane-1,3-dione | HCID 86694314 | 73.6% |
Reaction Steps
Under a nitrogen atmosphere, to a solution of 4.95 g of tert-butyl 2-(4-bromo-2-nitrobenzoyl)-3-oxobutanoate in 30 mL of dichloromethane was added 20 mL of trifluoroacetic acid under ice-cooling. The mixture was warmed to room temperature and stirred for 2.5 hours, and then the solvent was evaporated under reduced pressure. To the residue was added ethyl acetate, and the solution was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 2.7 g of 1-(4-bromo-2-nitrophenyl)butane-1,3-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822448B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-8af8931798734c489dbb562b145b2b07 |
| Source note | uspto-grants-2014_09 |