HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (4-Hydroxyphenyl)diphenylsulfonium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | (4-Methoxyphenyl)diphenylsulfonium triflate | HCID 11619123 | — |
| Reactant | Boron tribromide dichloromethane | HCID 22277759 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-Hydroxyphenyl)diphenylsulfonium chloride | HCID 18411308 | — |
Reaction Steps
To a methylene chloride solution of 20 g of the diphenyl-4-methoxyphenylsulfonium trifluoromethanesulfonate, 90 ml of a 1 M boron tribromide-methylene chloride solution was slowly dropwise added with stirring at room temperature, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture formed, methanol and distilled water were slowly added, followed by drying under reduced pressure to obtain a white crystal compound. The white crystal compound was dissolved in methanol, and ion exchange was effected using an anionic ion-exchange resin (Cl− type), followed by drying under reduced pressure to obtain 11.5 g of diphenyl-4-hydroxyphenylsulfonium chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06468714B2 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-eaf75bf8c42643fe809aa8a81c396d20 |
| Source note | uspto-grants-2002_10 |