HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl sulfoxide → Triphenylsulfonium Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl sulfoxide | HCID 13679 | — |
| Reactant | Bromhydrol | HCID 166749 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Triphenylsulfonium Bromide | HCID 11984010 | 128.2% |
Reaction Steps
In 200 ml of benzene were dissolved 21.1 g (0.1 mol) of diphenylsulfoxide, and 160.0 g (0.6 mol) of aluminum bromide at room temperature were added thereto, followed by allowing to react at 80° C. for 2 hours with stirring. The reaction solution was poured into 1000 ml of ice and extracted 3 times with methylene chloride. Thus obtained organic layer was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure to give 22.0 g (yield: 64%) of triphenylsulfonium bromide as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924323B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-cf2c1b4f48284176a14681a74edf5a2c |
| Source note | uspto-grants-2005_08 |