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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfone | HCID 6213 | — |
| Reactant | 2-Fluoro-4-methoxybenzoyl chloride | HCID 14484714 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Fluoro-4-methoxyphenyl)-2-(methylsulfonyl)ethanone | HCID 64018241 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889711B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-e21e3085a0774f6ea1f6a21382f2eb24 |
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| Source note | uspto-grants-2014_11 |
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