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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113826Generated: November 2, 2026

Trifluoroacetic acid → 3-(6-Ethanesulfonyl-pyridin-3-yloxy)-5-hydroxybenzoic acid methyl ester

https://huagongshe.com/reaction/2113826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-(6-Ethanesulfonyl-pyridin-3-yloxy)-5-methoxymethoxybenzoic acid methyl esterHCID 68711944—
SolventDichloromethaneHCID 6344—
Product3-(6-Ethanesulfonyl-pyridin-3-yloxy)-5-hydroxybenzoic acid methyl esterHCID 5475401485%

Reaction Steps

After adding 30.0 ml of trifluoroacetic acid to a solution of 11.8 g (30.9 mmol) of the obtained ester compound in methylene chloride (50.0 ml), the reaction mixture was stirred at room temperature for 5 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 =2:1) to obtain 8.86 g of 3-(6-ethanesulfonyl-pyridin-3-yloxy)-5-hydroxybenzoic acid methyl ester (yield: 85%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432287B2
Source datasetuspto-grants-2008_10
ORD IDord-910776ec12e74521a7577b3f7bd638a6
Source noteuspto-grants-2008_10