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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120534Generated: November 2, 2026

Triphenylsulfonium chloride → HCID 23435182, compound

https://huagongshe.com/reaction/2120534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantHCID 23712171HCID 23712171—
SolventDichloromethaneHCID 6344—
ProductHCID 23435182HCID 2343518243%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06692893B2
Source datasetuspto-grants-2004_02
ORD IDord-8f158619dede4ee7978e7895e8b5de7d
Source noteuspto-grants-2004_02