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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30741Generated: October 28, 2026

Hydrochloric Acid → Methyl 2-methoxy-4-trifluoromethane-sulfonyloxybenzoate

https://huagongshe.com/reaction/30741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantMethyl 4-hydroxy-2-methoxybenzoateHCID 12532676—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-methoxy-4-trifluoromethane-sulfonyloxybenzoateHCID 23282575—

Reaction Steps

Trifluoromethanesulfonic anhydride (2.24 mL) was added to an ice-cooled mixture of methyl 4-hydroxy-2-methoxybenzoate (2.02 g) and pyridine (0.14 mL) in methylene chloride (15 mL) with stirring. The mixture was stirred at room temperature for 30 min, and poured into a mixture of hydrochloric acid and ethyl acetate. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford methyl 2-methoxy-4-trifluoromethanesulfonyloxybenzoate (3.49 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423185B2
Source datasetuspto-grants-2008_09
ORD IDord-887166da898c4f14ba6a5603f09da6c5
Source noteuspto-grants-2008_09