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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061303Generated: October 26, 2026

(p-Hydroxyphenyl)diphenylsulfonium trifluoromethanesulfonate → Benzoic acid-2,2-difluoro-2-sulfo-ethyl ester diphenyl-4-hydroxyphenylsulfonium salt

https://huagongshe.com/reaction/2061303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(p-Hydroxyphenyl)diphenylsulfonium trifluoromethanesulfonateHCID 22389942—
ReactantBenzoic acid-2,2-difluoro-2-sulfo-ethyl ester sodium saltHCID 131729980—
SolventWaterHCID 962—
ProductBenzoic acid-2,2-difluoro-2-sulfo-ethyl ester diphenyl-4-hydroxyphenylsulfonium saltHCID 13172997956.4%

Reaction Steps

About 6 g of the diphenyl-4-hydroxyphenylsulfonium trifluoromethanesulfonate salt manufactured in the synthesis example 3 and about 4.84 g of a benzoic acid-2,2-difluoro-2-sulfo-ethyl ester sodium salt were dissolved in about 100 ml of an MC and about 100 ml of water, and a synthesis reaction (see Equation 9 below) was performed while strongly stirring for about three hours. In this instance, a process of the synthesis reaction was observed by 19F NMR using a small amount of an extracted organic phase. The organic phase was extracted when the synthesis reaction was terminated, and washed using the MC of a soluble solvent and hexane of a sparingly soluble solvent. Next, the solvents were removed, and drying under a reduced pressure was performed to obtain about 4.3 g (a yield: about 56.4%) of a benzoic acid-2,2-difluoro-2-sulfo-ethyl ester diphenyl-4-hydroxyphenylsulfonium salt, and a structure of the benzoic acid-2,2-difluoro-2-sulfo-ethyl ester diphenyl-4-hydroxyphenylsulfonium salt was observed by 1H-NMR (see FIG. 8):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283102B2
Source datasetuspto-grants-2012_10
ORD IDord-9744f832b15d4811b24d42a015fcb37a
Source noteuspto-grants-2012_10