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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028434Generated: November 2, 2026

Hydrogen Peroxide → 5-Tert-butyl-1-methanesulphinyl-2-methoxy-3-nitro-benzene

https://huagongshe.com/reaction/1028434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant5-(tert-Butyl)-2-methoxy-3-nitroanilineHCID 11206863—
Reactant5-Tert-butyl-2-methoxy-1-methylsulphanyl-3-nitro-benzeneHCID 58493929—
Solvent1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
Product5-Tert-butyl-1-methanesulphinyl-2-methoxy-3-nitro-benzeneHCID 58493951—

Reaction Steps

At ambient temperature 1.1 ml of a 35% aqueous hydrogen peroxide solution are added to a solution of 500 mg 5-tert-butyl-2-methoxy-1-methylsulphanyl-3-nitro-benzene (may be obtained starting from 5-tert-butyl-2-methoxy-3-nitro-aniline analogously to the method described in Syn. Commun. 1984, 14, 215-8 or in Syn. Commun. 2001, 31, 1857-62) in 15 ml of 1,1,1,3,3,3-hexafluoroisopropanol. The solution is stirred for 5 h at ambient temperature and then quenched with 10% aqueous Na2S2O3 solution. The resulting mixture is extracted with ethyl acetate, and the combined extracts are washed with saturated aqueous NaHCO3 solution and saturated aqueous saline solution. The organic phase is dried (Na2SO4) and the solvent is distilled off. The residue is chromatographed on silica gel with petroleum ether/ethyl acetate (20:1) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735579B2
Source datasetuspto-grants-2014_05
ORD IDord-52b78f252e924ab89c6f381bdc648b4d
Source noteuspto-grants-2014_05