HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → [(2-Methoxy-6-methylphenyl)methyl](triphenyl)phosphanium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,3-Dimethylanisole | HCID 76269 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | [(2-Methoxy-6-methylphenyl)methyl](triphenyl)phosphanium bromide | HCID 71323067 | 61.5% |
Reaction Steps
After 4.34 g of N-bromosuccinimide and 0.54 g of benzoyl peroxide were added to a solution of 3.03 g of 2,3-dimethylanisole in 70 ml of carbon tetrachloride, the mixture was heated under reflux for 30 minutes. After cooling, insoluble solid in the reaction mixture were filtered off and the filtrate was concentrated under reduced pressure to give an oil. The obtained oil was dissolved in 50 ml of benzene, and 5.82 g of triphenylphosphine was added to the solution. The mixture was heated under reflux for 11 hours. After cooling, the precipitated crystals were collected by filtration and recrystallized from methylene chloride-benzene to give 6.51 g of (2-methoxy-6-methylbenzyl)(triphenyl)phosphonium bromide as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044206B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-0e509fef62494341913bfd5e189bd3d0 |
| Source note | uspto-grants-2011_10 |