HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylsulfonium chloride → HCID 23435187, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | HCID 23712170 | HCID 23712170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23435187 | HCID 23435187 | 76% |
Reaction Steps
The sodium 4-(4′-methylphenylsulfonyloxy)naphthalene-1-sulfonate crude product obtained in Synthesis Example 2, 48 g, was added to one half of the aqueous triphenylsulfonium chloride solution obtained in Synthesis Example 4 and 200 g of dichloromethane, which was stirred for one hour at room temperature. The organic layer was separated, washed with 200 g of water, and concentrated in vacuum. The residue, 60 g, was purified by recrystallization from diethyl ether, obtaining the end product, triphenylsulfonium 4-(4′-methylphenylsulfonyloxy)naphthalene-1-sulfonate as crystals in an amount of 49 g (yield 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06692893B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-2d695418e6354faaac3caced887a974e |
| Source note | uspto-grants-2004_02 |