HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-(4-Chlorobenzoyl)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-3'-methylbenzophenone | HCID 2757666 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(4-Chlorobenzoyl)benzyl bromide | HCID 13649653 | 57.2% |
Reaction Steps
A mixture of 3-(4-chlorobenzoyl)toluene (5.48 g, 23.7 mmol) and dibenzoylperoxide (100 mg, 0.413 mmol) in carbon tetrachloride (45 ml) was treated with N-bromosuccinimide (4.65 g, 26.7 mmol) and refluxed 2.5 hours. The mixture was filtered while hot and slowly cooled to ambient temperature. The precipitate was collected by filtration, washed twice with carbon tetrachloride, and dried under vacuum to provide 4.2 g (57%) of 3-(4-chlorobenzoyl)benzyl bromide, m.p. 123°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04590201 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-def8e9af73b044d3a6471a3d3f9b9c5a |
| Source note | uspto-grants-1986_05 |