HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 3-(1-Bromoethyl)benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Ethylbenzophenone | HCID 583730 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(1-Bromoethyl)benzophenone | HCID 12802924 | — |
Reaction Steps
Into a 200 ml reactor equipped with a reflux condenser and a stirrer, 60 ml of carbon tetrachloride and 10 g of 3-ethylbenzophenone were introduced. While stirring the resultant mixture at room temperature, 8.6 g of N-bromosuccinimide and 0.14 g of benzoyl peroxide were added thereto, and reflux was performed for 8 hours while stirring the reaction solution. After the reaction solution had been cooled to room temperature, the succinimide was filtered out, and carbon tetrachloride was distilled off from a filtrate under a reduced pressure. The spectrum data of the obtained product were in accord with those of 3-(1-bromoethylbenzophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761508 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-808cbc7c67484e6e8b9a7ce6224107ab |
| Source note | uspto-grants-1988_08 |