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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336827Generated: October 30, 2026

Hydrochloric Acid → 1-(2-Fluoro-4-methoxyphenyl)-2-(methylsulfonyl)ethanone

https://huagongshe.com/reaction/336827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoneHCID 6213—
Reactant2-Fluoro-4-methoxybenzoyl chlorideHCID 14484714—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Fluoro-4-methoxyphenyl)-2-(methylsulfonyl)ethanoneHCID 6401824146%

Reaction Steps

To a solution of 4.15 g (44.07 mmol) of dimethylsulfone in 140 ml of anhydrous tetrahydrofuran are added dropwise at −10° C. under argon 24 ml of methyllithium solution (1.6M in diethyl ether, 38.2 mmol). The reaction mixture is stirred for 15 min at room temperature, the reaction mixture is then cooled to −60° C. A solution of 5.54 g (29.38 mmol) of 2-fluoro-4-methoxybenzoyl chloride dissolved in 60 ml of tetrahydrofuran is then added dropwise to the reaction mixture. This mixture is stirred for 4 h at between −60° C. and 0° C., then a 1M hydrochloric acid solution is added. The product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate and concentrated. The residue is triturated in minimum methanol and the solid is filtered to yield 3.33 g (46%) of 1-(2-fluoro-4-methoxyphenyl)-2-(methylsulfonyl)ethanone in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889711B2
Source datasetuspto-grants-2014_11
ORD IDord-e21e3085a0774f6ea1f6a21382f2eb24
Source noteuspto-grants-2014_11