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HRID 1033111Erstellt: 26. Oktober 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/1033111

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl iodideHCID 10962—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 4-[(2-butyl-5-formyl-1H-imidazol-1-YL)methyl]benzoateHCID 10334966—
EduktDiethyl (2,5-dioxo-2,5-dihydro-1H-imidazol-4-yl)phosphonateHCID 53733419—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl Z-4-[[2-butyl-5-[(1-butyl-2,5-dioxo-4-imidazolidinylidene)methyl]-1H-imidazol-1-yl]methyl]benzoateHCID 11743857—

Reaktionsschritte

To a solution of diethyl 2,5-dioxo-4-imidazolylphosphonate (1.5 g, 0.33 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05308853
Quelldatensatzuspto-grants-1994_05
ORD IDord-d6ec9288e119447dbbac5aa643d34671
Quellennotizuspto-grants-1994_05