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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648511Generated: October 25, 2026

Butyl iodide → Methyl Z-4-[[2-butyl-5-[(1-butyl-2,5-dioxo-4-imidazolidinylidene)methyl]-1H-imidazol-1-yl]methyl]benzoate

https://huagongshe.com/reaction/1648511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-[(2-butyl-5-formyl-1H-imidazol-1-YL)methyl]benzoateHCID 10334966—
ReactantDiethyl (2,5-dioxo-2,5-dihydro-1H-imidazol-4-yl)phosphonateHCID 53733419—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl Z-4-[[2-butyl-5-[(1-butyl-2,5-dioxo-4-imidazolidinylidene)methyl]-1H-imidazol-1-yl]methyl]benzoateHCID 11743857—

Reaction Steps

To a solution of diethyl 2,5-dioxo-4-imidazolylphosphonate (1.5 g, 6.33 mmol) in DMF (4 mL) is added K2CO3 and then 1-iodobutane (0.79 mL, 6.96 mmol). This mixture is stirred for 16 hours at room temperature. To this yellow mixture is added methyl 4-[(2-butyl-5-formyl-1H-imidazol-1-yl)methyl]benzoate (1.05 g, 3.5 mmol). After 2 hours methylene chloride (10 mL) was added to aid stirring. The mixture was stirred for 16 hours. After diluting the reaction mixture with water it was extracted with ethyl acetate. This extract was washed with water and brine. The extract was dried over MgSO4,filtered and then concentrated until crystallization was apparent. The solid was collected and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436260
Source datasetuspto-grants-1995_07
ORD IDord-dc9ce36a57964e8c8b682cc096803689
Source noteuspto-grants-1995_07