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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857688Generated: November 2, 2026

Sodium hydride → 5-(3,5-dimethylphenylthio)-4-isopropyl-1H-imidazole

https://huagongshe.com/reaction/1857688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3,5-DimethylbenzenethiolHCID 117548—
Reactant4-isopropyl-5-iodo-1H-imidazoleHCID 178440197—
SolventDimethylformamideHCID 6228—
Product5-(3,5-dimethylphenylthio)-4-isopropyl-1H-imidazoleHCID 17842533753%

Reaction Conditions

Temperature140 °C

Reaction Steps

In 30 ml of dry N,N-dimethylformamide was dissolved 4.0 g (16.9 mmol) of 4-isopropyl-5-iodo-1H-imidazole (4b), followed by addition of 4.68 g (33.9 mmol) of 3,5-dimethylthiophenol and 2.1 g (52.5 mmol) of 60% sodium hydride. The mixture was heated at 140° C. for 7 hours. The N,N-dimethylformamide was there distilled off under reduced pressure and, after addition of dry ice, the residue was extracted with methylene chloride. The organic layer was washed with water and dried over sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was fractionated by silica gel chromatography (3% methanol-methylene chloride). The eluted crude compound was recrystallized from ethyl acetate-diisopropyl ether to provide 2.2 g (yield 53%) of 5-(3,5-dimethylphenylthio)-4-isopropyl-1H-imidazole (X=Y=Me) (9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147097
Source datasetuspto-grants-2000_11
ORD IDord-3b70644359ae4c70b4c9b908698e1da8
Source noteuspto-grants-2000_11