HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylsulfonium chloride → HCID 23435182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | HCID 23712171 | HCID 23712171 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23435182 | HCID 23435182 | 43% |
Reaction Steps
The sodium 8-(4′-methylphenylsulfonyloxy)naphthalene-1-sulfonate crude product obtained in Synthesis Example 3, 26 g, was added to a quarter of the aqueous triphenylsulfonium chloride solution obtained in Synthesis Example 4 and 100 g of dichloromethane, which was stirred for one hour at room temperature. The organic layer was separated, washed with 100 g of water, and concentrated in vacuum. The residue, 32 g, was purified by recrystallization from diethyl ether, obtaining the end product, triphenylsulfonium 8-(4′-methylphenylsulfonyloxy)naphthalene-1-sulfonate as crystals in an amount of 25 g (yield 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06692893B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-8f158619dede4ee7978e7895e8b5de7d |
| Source note | uspto-grants-2004_02 |