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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354995Generated: October 31, 2026

Ethyl Acetate → 3-(3-Fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl ester

https://huagongshe.com/reaction/2354995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium methanesulfinateHCID 2733271—
Reactant3-(4-Bromo-3-fluoro-phenoxy)-5-methoxymethoxybenzoic acid methyl esterHCID 68708471—
Reactantbrine NH4OHHCID 131727087—
CatalystCopper iodideHCID 83717—
SolventDimethyl SulfoxideHCID 679—
Product3-(3-Fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl esterHCID 6870471448%

Reaction Conditions

Temperature120 °C

Reaction Steps

After adding 757 mg (7.41 mmol) of sodium methanesulfinate and 1.41 g (7.41 mmol) of copper iodide to a solution of 357 mg (0.93 mmol) of the obtained ester compound in dimethylsulfoxide (6.0 ml), the reaction mixture was stirred at 120° C. for 6 hours. Sodium chloride water-ammonia water (9:1) was added to the reaction mixture and extraction was performed with acetic acid ethyl ester, and then the organic layer was washed with brine, dried and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=2:1) to obtain 170 mg of 3-(3-fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl ester (yield: 48%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754743B2
Source datasetuspto-grants-2010_07
ORD IDord-fb3c77bbe7944fc1b8fa9abe353f6c0d
Source noteuspto-grants-2010_07