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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539938Generated: October 27, 2026

Methyl iodide → 4-Nitrophenyl methyl sulfide

https://huagongshe.com/reaction/539938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant4-NitrobenzenethiolHCID 15809—
SolventWaterHCID 962—
Product4-Nitrophenyl methyl sulfideHCID 9610950.4%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a suspension of p-nitrothiophenol (20 g, 0.129 mol) in water (150 mL) was added an aqueous solution of sodium hydroxide (75 mL, 2 N) at room temperature. After the mixture was stirred for 15 minutes and cooled to 10° C., methyl iodide (57 g, 25 mL, 0.401 mol) was added slowly. The reaction mixture was allowed to warm to room temperature and stirred for 2.5 hours. The resulting mixture was extracted with diethyl ether (100 mL×3). The organic layers were combined, washed with water (200 mL) and brine (200 mL), dried over calcium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography to afford 11 g of 1-(methylsulfanyl)-4-nitrobenzene as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-d7ccfdfe81114b4f9d7cad3ce0991d41
Source noteuspto-grants-2014_10