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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199393Generated: October 27, 2026

1,2,3,4-Tetramethylbenzene → (Chloromethyl)(2,3,4,5-tetramethylphenyl)(p-tolyl)sulfonium triflate

https://huagongshe.com/reaction/2199393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetramethylbenzeneHCID 10263—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant1-[(Chloromethyl)sulfinyl]-4-methylbenzeneHCID 11127044—
SolventDiethyl EtherHCID 3283—
Product(Chloromethyl)(2,3,4,5-tetramethylphenyl)(p-tolyl)sulfonium triflateHCID 131735041—

Reaction Steps

1-((chloromethyl)sulfinyl)-4-methylbenzene (500 mg, 2.65 mmol) of example 29 was dissolved in dry diethyl ether (5 mL) under an argon atmosphere. 1,2,3,4-Tetramethylbenzene (0.40 mL, 1 eq) was slowly added to the previous solution and then the mixture was cooled to a temperature between 5° C. and 0° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.45 mL, 1 eq) was added maintaining the same temperature. The mixture was stirred until the reaction was complete. The precipitated triflate salt was isolated by filtration and washed with diethyl ether (5 mL) at 0° C. 1.12 g (89.74%) of the desired product was obtained as a white solid. Mp=28-30° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359294B2
Source datasetuspto-grants-2016_06
ORD IDord-984105186cd74700975addee864213db
Source noteuspto-grants-2016_06