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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199396Generated: October 29, 2026

1,2,3,4-Tetramethylbenzene → (Bromomethyl)(phenyl)(2,3,4,5-tetramethylphenyl)sulfonium triflate

https://huagongshe.com/reaction/2199396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetramethylbenzeneHCID 10263—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantBromomethyl phenyl sulfoxideHCID 11816834—
SolventDiethyl EtherHCID 3283—
Product(Bromomethyl)(phenyl)(2,3,4,5-tetramethylphenyl)sulfonium triflateHCID 87429207—

Reaction Steps

Bromomethyl phenyl sulfoxide (500 mg, 2.29 mmol) of example 32 was dissolved in dry diethyl ether (15 mL) under an argon atmosphere. 1,2,3,4-Tetramethylbenzene (339 mg, 1.09 eq) was added to the previous solution and then the mixture cooled to a temperature below −60° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.385 ml, 1.0 eq) was added slowly, maintaining the same temperature. The mixture was stirred until the reaction was complete. The precipitated triflate salt formed was isolated by filtration, washed with diethyl ether at 0° C. and dried under vacuum. 0.779 g (70%) of the desired product was obtained as a white solid. mp: 115-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359294B2
Source datasetuspto-grants-2016_06
ORD IDord-0255c102b80c4c1482c3e2ff298f7d28
Source noteuspto-grants-2016_06