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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585464Generated: November 1, 2026

Pyridine → Methyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoate

https://huagongshe.com/reaction/1585464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantMethyl 3-hydroxy-4-methanesulfonyl-2-methylbenzoateHCID 18694846—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoateHCID 1869485799.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

8.8 g (0.036 mol) of methyl 3-hydroxy-4-methanesulfonyl-2-methyl-benzoate was dissolved in 100 ml of methylene chloride, and 8.3 g (0.11 mol) of pyridine was added. After the solution was cooled to 0° C., 12.2 g (0.043 mol) of anhydrous trifluoromethanesulfonic acid was added. After stirring at room temperature for 1 hour, the reaction mixture was washed with 1N hydrochloric acid and subsequently with saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 13.5 g of methyl 4-methanesulfonyl-2-methyl-3-(trifluoromethanesulfonyl)oxybenzoate. Yield=99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939360
Source datasetuspto-grants-1999_08
ORD IDord-7719549e4b174447b74d31accaeae9a0
Source noteuspto-grants-1999_08