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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407870Generated: October 25, 2026

Methyl iodide → 1,2,4-Trifluoro-5-(methylsulfonyl)benzene

https://huagongshe.com/reaction/407870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4,5-Trifluorobenzenesulfinic acidHCID 57241375—
SolventDimethylformamideHCID 6228—
Product1,2,4-Trifluoro-5-(methylsulfonyl)benzeneHCID 4673939671.1%

Reaction Steps

To a solution of 2,4,5-trifluorobenzenesulfinic acid (34 g, 173 mmol), in DMF (200 mL), was added iodomethane (21.6 mL, 347 mmol), and N-ethyl-N-isopropylpropan-2-amine (60.5 mL, 347 mmol). The reaction mixture was stirred overnight at ambient temperature. The reaction was concentrated and partitioned between water and ethyl acetate and extracted with CH2Cl2. The combined organic layers were concentrated and purified over silica gel (15-100% EtOAc in hexanes) to afford 1,2,4-trifluoro-5-(methylsulfonyl)benzene (25.8 g, 123 mmol, 71% yield) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-4d3484d721434e5da22963726d069d9d
Source noteuspto-grants-2014_06