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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027855Generated: November 3, 2026

Sodium Chloride → 1-(Ethylsulfanyl)-4-nitrobenzene

https://huagongshe.com/reaction/1027855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantIodoethaneHCID 6340—
ReactantSodium HydroxideHCID 14798—
Reactant4-NitrobenzenethiolHCID 15809—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(Ethylsulfanyl)-4-nitrobenzeneHCID 1232133986.2%

Reaction Steps

16.56 g (106.72 mmol) of 4-nitrothiophenol was added, while cooling with water, to a solution of 4.27 g (106.76 mmol) sodium hydroxide in 320 ml ethanol and it was stirred for 15 minutes at room temperature. Then, while cooling with water, 8.63 ml (106.79 mmol) of ethyl iodide was added and the mixture was stirred overnight at room temperature. The mixture was added to saturated sodium chloride solution and was extracted with ethyl acetate (2×). The combined organic phases were dried (Na2SO4), filtered and concentrated by evaporation. Then it was dissolved in DCM and filtered again and evaporated to dryness. 16.86 g (92.02 mmol) of the raw product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735412B2
Source datasetuspto-grants-2014_05
ORD IDord-298dec004d194a428acb527faaae0ef4
Source noteuspto-grants-2014_05