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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080349Generated: November 1, 2026

Triphenylsulfonium chloride → Triphenylsulfonium hydroxycarbonyldifluoromethanesulfonate

https://huagongshe.com/reaction/2080349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantSodium difluorosulfoacetateHCID 86607434—
ProductTriphenylsulfonium hydroxycarbonyldifluoromethanesulfonateHCID 86613393—

Reaction Steps

Into 2036 parts of 11.2% aqueous triphenylsulfonium chloride solution, 859 parts of 17.6% aqueous sodium difluorosulfoacetate solution was added and the resultant mixture was stirred at 25° C. for about 20 hours. The mixture was filtered to obtain white solid and white solid obtained was washed with 150 parts of ion-exchanged water. 506 Parts of tert-butyl methyl ether was added to white solid obtained. The resultant mixture was stirred and filtered to obtain solid. The solid obtained was dried to obtain 246.9 parts of triphenylsulfonium hydroxycarbonyldifluoromethanesulfonate, which is called as TPS-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932334B2
Source datasetuspto-grants-2011_04
ORD IDord-6f0894cc11c94e068617ca9f1fd40f49
Source noteuspto-grants-2011_04