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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415984Generated: November 2, 2026

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

https://huagongshe.com/reaction/1415984

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 then 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 numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-d8c2edc9f1c149878fddd0e5fe01d81d
Source noteuspto-grants-1999_06