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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228006Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → Methyl 2-trifluoromethylsulfonyloxy-4-methylbenzoate

https://huagongshe.com/reaction/2228006

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 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 numberUS06414145B1
Source datasetuspto-grants-2002_07
ORD IDord-cf7a0885c1cd4a0ba636aead7fd32016
Source noteuspto-grants-2002_07