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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507398Generated: October 25, 2026

Potassium Carbonate → 4-[2-(2-Methyl-5-oxo-4,4-diphenyl4,5-dihydro-imidazol-1-yl)-acetyl]-benzoic acid ethyl ester

https://huagongshe.com/reaction/507398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-methyl-4,4-diphenyl-1H-imidazol-5-oneHCID 619503—
ReactantEthyl 4-(2-bromoacetyl)benzoateHCID 11966043—
ReactantCyclohexane ethylacetateHCID 21867204—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product4-[2-(2-Methyl-5-oxo-4,4-diphenyl4,5-dihydro-imidazol-1-yl)-acetyl]-benzoic acid ethyl esterHCID 6846405348.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 4-(2-bromo-acetyl)-benzoic acid ethyl ester (812 mg, 3 mmol) and 2-methyl-5,5-diphenyl-3,5-dihydro-imidazol-4-one (750 mg, 3 mmol) in 12 mL acetone, potassium carbonate (502 mg, 3.6 mmol) is added and the reaction mixture is heated at 70° C. for 5 min in the microwave oven (Biotage Initiator). The mixture is cooled to room temperature, filtered and the filtrate evaporated to yield the crude product which is subjected to flash chromatography. ISCO Companion CombiFlash, 80 g silica gel, cyclohexane/ethyl acetate, gradient, ethyl acetate 0-100% to yield 4-[2-(2-methyl-5-oxo-4,4-diphenyl4,5-dihydro-imidazol-1-yl)-acetyl]-benzoic acid ethyl ester (635 mg, 45%) as light yellow solid. LC/MS at 254 nm; [M+H] 441; Rt 3.613 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786155B2
Source datasetuspto-grants-2010_08
ORD IDord-f9d8a6508a3d42dbae724ee41ebb2115
Source noteuspto-grants-2010_08