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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113823Generated: October 25, 2026

Trifluoroacetic acid → Methyl 3-hydroxy-5-(4-(methylsulfonyl)phenoxy)benzoate

https://huagongshe.com/reaction/2113823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl esterHCID 59263314—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-hydroxy-5-(4-(methylsulfonyl)phenoxy)benzoateHCID 4694184656%

Reaction Steps

After adding 60 ml of trifluoroacetic acid to a solution of 30.9 g (84.3 mmol) of the obtained 3-(4-methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester in methylene chloride (100 ml) while cooling on ice, the reaction mixture was stirred at room temperature for 4 hours. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=1:1) to obtain 15.2 g of 5-hydroxy-3-(4-methanesulfonyl-phenoxy)benzoic acid methyl ester (yield: 56%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432287B2
Source datasetuspto-grants-2008_10
ORD IDord-1f6b4700085c4bc0a33456e44ff292b5
Source noteuspto-grants-2008_10