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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228367Generated: October 29, 2026

Triphenylsulfonium chloride → HCID 18469754, compound

https://huagongshe.com/reaction/2228367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantHCID 18469740HCID 18469740—
SolventDichloromethaneHCID 6344—
ProductHCID 18469754HCID 1846975452%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06416928B1
Source datasetuspto-grants-2002_07
ORD IDord-d0a27f17fca4480caf5f5daaf7dce84c
Source noteuspto-grants-2002_07