HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 20330252, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 20330256 | HCID 20330256 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 20330252 | HCID 20330252 | — |
Reaction Steps
A mixture of 10.5 g (0.046 mole) 1-(5-chloro-2-pyridinyloxy)-3,3-dimethyl-2-butanone, prepared above, and 8.37 g (0.047 mole) N-bromosuccinimide (NBS) in 300 ml. carbon tetrachloride, with stirring, was irradiated and heated with a sunlamp until all of the NBS was consumed (about 45 min.). The reaction mixture was cooled, filtered, and the filtrate washed with aqueous sodium bisulfite and dried. After removal of the solvent, there was obtained a quantitative yield of 1-bromo-1-(5-chloro-2-pyridinyloxy)-3,3-dimethyl-2-butanone, a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166854 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-062bb4e904fe4a3784b1f7ab9013ff1f |
| Source note | uspto-grants-1979_09 |