HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylsulfonium chloride → HCID 18469754, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | HCID 18469740 | HCID 18469740 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18469754 | HCID 18469754 | 52% |
Reaction Steps
The 4-phenylmethylbenzenesulfonic acid crude product obtained in Synthesis Example 1 was added to the aqueous triphenylsulfonium chloride solution obtained in Synthesis Example 2 and 90 g of dichloromethane, which was stirred for one hour at room temperature. The organic layer was separated, washed with 100 g of water, and evaporated in vacuum. The residue, 27 g, was purified by silica gel column chromatography (eluent, dichloromethane/methanol), obtaining the end product, triphenylsulfonium 4-phenylmethylbenzenesulfonate. It was 21 g (yield 52%) of an oily matter containing a minor amount of solvents (methanol, etc.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06416928B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-d0a27f17fca4480caf5f5daaf7dce84c |
| Source note | uspto-grants-2002_07 |