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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238129Generated: October 25, 2026

Sodium Thiosulfate → 1-(Methylsulfinyl)-4-nitrobenzene

https://huagongshe.com/reaction/238129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantMetaperiodic acidHCID 65185—
Reactant4-Nitrophenyl methyl sulfideHCID 96109—
CatalystIron chloride (FeCl3)HCID 24380—
SolventAcetonitrileHCID 6342—
Product1-(Methylsulfinyl)-4-nitrobenzeneHCID 305882—

Reaction Steps

A suspension of 25.0 g (147.8 mmol) 1-methylsulfanyl-4-nitro-benzene and 0.69 g (4.2 mmol) iron(III) chloride (anhydrous) in 120 ml acetonitrile is treated with 36.0 g (158.1 mmol) periodic acid and stirred at room temperature. At the start of heat evolution, the mixture is transiently cooled with an ice-bath, so that the temperature does not rise above 30° C. After the heat evolution has subsided, the mixture is stirred at room temperature for a further 10 mins. The mixture is poured into a solution of 150 g sodium thiosulphate in 1000 ml ice-water and then extracted with DCM. The combined organic phases are washed with saturated NaCl solution, dried (Na2SO4), filtered and concentrated. The remaining residue is recrystallised from toluene. 23.6 g (128.0 mmol, corresponding to 86% of theor.) of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642611B2
Source datasetuspto-grants-2014_02
ORD IDord-52488375d7e24f31be2d2617bf4cd6b3
Source noteuspto-grants-2014_02