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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251863Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → Methyl 2-trifluoromethylsulfonyloxy-4-methylbenzoate

https://huagongshe.com/reaction/1251863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantBenzoic acid, 2-hydroxy-4-methyl-, methyl esterHCID 78400—
SolventPyridineHCID 1049—
ProductMethyl 2-trifluoromethylsulfonyloxy-4-methylbenzoateHCID 1847457690%

Reaction Steps

Triflic anhydride (170 ml; 1.01 mol) was added to a solution of methyl 2-hydroxy-4-methylbenzoate (153 g; 0.92 mol) in pyridine (1.5 l), at 0° C., The mixture was stirred at ambient temperature overnight. After evaporation of the pyridine, the residue was acidified to pH 3.5 with 6N HCl and extracted with ether. The organic phase was evaporated and the residue purified by flash column chromatography eluting with a gradient of 0-5% ethyl acetate/petroleum ether to give methyl 2-trifluoromethylsulfonyloxy-4-methylbenzoate (245 g; 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342765B1
Source datasetuspto-grants-2002_01
ORD IDord-48e90b10d89b4e44a278b461139c376e
Source noteuspto-grants-2002_01