HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1-Phenyl-3-(o-anisyloxy)propylbromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Methoxy-2-[(3-phenylpropoxy)methyl]benzene | HCID 15208420 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-Phenyl-3-(o-anisyloxy)propylbromide | HCID 20336045 | — |
Reaction Steps
Using a similar procedure to that above, a reaction mixture was prepared containing 48 g. of N-bromosuccinimide, 65 g. of 1-phenyl-3-(o-anisyloxy)propane and 300 ml. of carbon tetrachloride. 500 mg. of benzoyl peroxide were added and the resulting mixture heated at reflux for about 2 hours at which point thin-layer chromatography indicated that no starting material remained in the reaction mixture. The reaction mixture was cooled, the succinimide separated by filtration and the solvent removed from the filtrate by evaporation in vacuo. A residual oil weighing about 88 g. comprising 1-phenyl-3-(o-anisyloxy)propylbromide formed in the above reaction was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04207343 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-4ac83b515d464eeabfe186be56067547 |
| Source note | uspto-grants-1980_06 |