HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69114Generated: October 29, 2026
Acetonitrile → 1-[2-Amino-5-bromo-4-(trifluoromethyl)phenyl]ethanone
https://huagongshe.com/reaction/69114
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(2-Amino-4-(trifluoromethyl)phenyl)ethan-1-one | HCID 46835500 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[2-Amino-5-bromo-4-(trifluoromethyl)phenyl]ethanone | HCID 66696135 | 64.7% |
Reaction Steps
To a mixture of 11.6 g of 1-[2-amino-4-(trifluoromethyl)phenyl]ethanone, 60 mL of acetonitrile, and 230 mL of diethyl ether was added 2.85 g of Amberlyst (registered trademark) 15, and 10.1 g of N-bromosuccinimide was added thereto in three times in an ice bath. After stirring for 30 minutes in an ice bath, the mixture was stirred at room temperature overnight. The insoluble material was filtered and washed with ethyl acetate. To the filtrate were added water and ethyl acetate, and the aqueous layer was separated. The organic layer was washed with a 10% aqueous sodium thiosulfate solution and saturated brine, and dried over anhydrous magnesium sulfate, and then solvent was evaporated. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 10.36 g of 1[2-amino-5-bromo-4-(trifluoromethyl)phenyl]ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08822448B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-195fbe543fdd481195764ad9f4a660d0 |
|---|
| Source note | uspto-grants-2014_09 |
|---|