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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120533Generated: November 1, 2026

Triphenylsulfonium chloride → HCID 23435187, compound

https://huagongshe.com/reaction/2120533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantHCID 23712170HCID 23712170—
SolventDichloromethaneHCID 6344—
ProductHCID 23435187HCID 2343518776%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06692893B2
Source datasetuspto-grants-2004_02
ORD IDord-2d695418e6354faaac3caced887a974e
Source noteuspto-grants-2004_02