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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571155Generated: November 1, 2026

Triphenylsulfonium Bromide → Triphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate

https://huagongshe.com/reaction/571155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium BromideHCID 11984010—
ReactantTriethylammonium 1,1-difluoro-2-(methacryloyloxy)ethanesulfonateHCID 86660800—
SolventChloroformHCID 6212—
ProductTriphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonateHCID 8664811087%

Reaction Steps

A 50 mL reactor was charged with the triethylammonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate aqueous solution obtained by the 3rd step, and a solution of 3.18 g (8.9 millimoles) of triphenylsulfonium bromide and 20 g of chloroform, followed by 3 hours of stirring at room temperature. Subsequently, an organic layer was separated, and the thus obtained organic layer was rinsed with 20 g of water four times. Subsequently, it was rinsed with 20 g of diisopropyl ether three times and then a volatile component was distilled off, thereby obtaining 3.92 g of a target triphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate. It exhibited a purity of 97% at this time, and a yield of 87% taken over from the 3rd step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024058B2
Source datasetuspto-grants-2015_05
ORD IDord-7a6d1b98f67a4b15876d1ce5bb9dfedd
Source noteuspto-grants-2015_05