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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30733Generated: October 28, 2026

Hydrochloric Acid → Benzyl 2-benzyloxy-4-trifluoromethanesulfonyloxybenzoate

https://huagongshe.com/reaction/30733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantBenzyl 2-benzyloxy-4-hydroxybenzoateHCID 23090785—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-benzyloxy-4-trifluoromethanesulfonyloxybenzoateHCID 23090750—

Reaction Steps

Trifluoromethanesulfonic anhydride (0.22 mL) was added to an ice-cooled mixture of benzyl 2-benzyloxy-4-hydroxybenzoate (0.40 g) and pyridine (0.1 mL) in methylene chloride (1.5 mL) with stirring, and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into a mixture of hydrochloric acid and ethyl acetate, and the 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, and the residue was purified by medium-pressure liquid silica gel column chromatography (eluent: n-hexane/ethyl acetate=6/1) to afford benzyl 2-benzyloxy-4-trifluoromethanesulfonyloxybenzoate (0.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423185B2
Source datasetuspto-grants-2008_09
ORD IDord-800e894c58404c6eb26e1575993b45cb
Source noteuspto-grants-2008_09