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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415986Generated: November 2, 2026

Dimethylformamide → 5-(3,5-Dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole-2-carbaldehyde

https://huagongshe.com/reaction/1415986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactant5-(3,5-dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazoleHCID 22130115—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product5-(3,5-Dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole-2-carbaldehydeHCID 47391473%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In 16 ml of dry tetrahydrofuran was dissolved 800 mg (3.1 mmol)of 5-(3,5-dimethylphenylthio)-4-isopropyl-1-methyl-1H-imidazole (X=Y=Me)(10). This solution was cooled to -78° C. and 2.2 ml of n-butyllithium-n-hexane (1.66 molar)was added dropwise under nitrogen. After 5 minutes, 680 mg (9.3 mmol) of dry N,N-dimethylformamide was added and the reaction was further conducted at the same temperature for 15 minutes. This reaction mixture was poured in ice-water and extracted with diethyl ether. 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 purified by silica gel chromatography (ethyl acetate:n-hexane=1:5)to provide 644 mg (yield 73%)of Compound I-6. mp 93 to 94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-fe984f0b2e01489593d96fc1565c718a
Source noteuspto-grants-1999_06