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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25459Generated: October 25, 2026

Monoperoxyphthalic Acid Magnesium Salt → 4-Fluoro-1-methylsulfinyl-2-nitrobenzene

https://huagongshe.com/reaction/25459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonoperoxyphthalic Acid Magnesium SaltHCID 10130449—
Reactant4-Fluoro-1-(methylsulfanyl)-2-nitrobenzeneHCID 12700911—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-Fluoro-1-methylsulfinyl-2-nitrobenzeneHCID 2256734663%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-Fluoro-1-methylsulfinyl-2-nitrobenzene can be obtained in the following way: 4.7 g of magnesium monoperoxyphthalate are added portionwise to a solution, under argon, of 1.9 g of 4-fluoro-1-methylsulfanyl-2-nitrobenzene in 6 ml of methanol and 30 ml of dichloromethane. The reaction mixture is then stirred at a temperature in the region of 20° C. for 3 hours, and is then filtered through sintered glass and the solid is washed with dichloromethane. The filtrate is washed with an aqueous sodium hydrogencarbonate solution then with water, dried over magnesium sulfate, treated with 3S black, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue thus obtained is purified by chromatography on a column of 125 g of silice (particle size 40-63 μm), eluting with pure dichloromethane. The fractions containing the expected product are pooled and concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. 1.3 g of 4-fluoro-1-methylsulfinyl-2-nitrobenzene are thus obtained in the form of a yellow foam (Rf=0.23, silica gel thin layer chromatography, eluent: dichloromethane/ethyl acetate 90/10)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858638B2
Source datasetuspto-grants-2005_02
ORD IDord-d3701a554f694506a5dba40497c51f19
Source noteuspto-grants-2005_02