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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087293Generated: October 29, 2026

Ethyl Acetate → Ethyl 3-oxo-3-(1-triphenylmethyl-1H-imidazol-4-yl)propionate

https://huagongshe.com/reaction/1087293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 1-trityl-1H-imidazole-4-carboxylateHCID 10429115—
SolventTolueneHCID 1140—
ProductEthyl 3-oxo-3-(1-triphenylmethyl-1H-imidazol-4-yl)propionateHCID 10002468—

Reaction Steps

202.65 g (0.55 mol) methyl (1-triphenylmethyl-1H-imidazol-4-yl)carboxylate are dissolved in 0.8 l dry toluene at 85° C. 44 g (1.1 mol) sodium hydride (60% dispersion in mineral oil) are added. To the stirred mixture 96.92 g (1.1 mol) ethyl acetate are dropped over 2 hours. The mixture is allowed to react 16 hours at 70° C. Subsequently the toluene is removed under reduced pressure. The resulting mixture is introduced into the following step without purification. For analytical purposes a small amount of the brown oily residue is dissolved in methylene chloride, washing with aqueous ammonium chloride solution and water, drying by means of sodium sulphate and evaporation lead to an oil. Crystallization with diethyl ether and recrystallization from ethanol/diethyl ether afford the title compound as white crystals, melting point 136°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034539
Source datasetuspto-grants-1991_07
ORD IDord-b2121c1251d94e318f010efb13ca9b17
Source noteuspto-grants-1991_07