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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113822Generated: October 25, 2026

Potassium Phosphate, Tribasic → 3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/2113822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Bromo-4-(methylsulphonyl)benzeneHCID 77014—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantMethyl 3-hydroxy-5-(methoxymethoxy)benzoateHCID 23136427—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl esterHCID 5926331471.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

After adding 33.4 g (142 mmol) of 4-methanesulfonyl-bromobenzene, 2.67 g (11.9 mmol) of palladium acetate, 5.31 g (17.8 mmol) of 2-(di-tert-butylphosphino)biphenyl and 50.3 g (237 mmol) of potassium phosphate to a solution of 25.0 g (119 mmol) of 5-hydroxy-3-methoxymethoxybenzoic acid methyl ester in toluene (375 ml), the reactor was sealed and the mixture was subsequently stirred at 130° C. for 6 hours. Acetic acid ethyl ester was added to the reaction mixture, which was then filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=2:1) to obtain 31.0 g of 3-(4-methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester (yield: 69%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432287B2
Source datasetuspto-grants-2008_10
ORD IDord-c299119bcbf2419e9ec0cb56e956bde2
Source noteuspto-grants-2008_10