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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076620Generated: November 1, 2026

Water → Methyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetate

https://huagongshe.com/reaction/2076620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantMethyl 4-hydroxy-3-methoxyphenylacetateHCID 85214—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetateHCID 8661740699.9%

Reaction Steps

Pyridine (2.10 ml, 25.9 mmol), anhydrous trifluoromethanesulfonic acid (1.61 ml, 9.53 mmol) and 4-dimethylaminopyridine (30 mg, 0.25 mmol) were added to a solution of methyl (4-hydroxy-3-methoxyphenyl)acetate (1.70 g, 8.66 mmol) in methylene chloride (20 ml) and the mixture was stirred under ice-cooling for 10 minutes and then stirred at room temperature for 20 minutes. After the reaction mixture was poured into water and the mixture was extracted with ethyl acetate, the organic layer was successively washed with water (twice) and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the solvent under reduced pressure was purified by silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=2/1) to give methyl (3-methoxy-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)acetate (2.84 g, yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-72801ca5016047b8bc0b45013c1383e6
Source noteuspto-grants-2011_04