Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825487Generated: October 31, 2026

Tetrahydrofuran → Ethyl 5-(2,4-dichlorophenyl)-4-imidazoly-5-oxopentanoate

https://huagongshe.com/reaction/1825487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcrylateHCID 8821—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(2,4-dichlorophenyl)-2-(1H-imidazol-2-yl)ethanoneHCID 22142718—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 5-(2,4-dichlorophenyl)-4-imidazoly-5-oxopentanoateHCID 57107536108%

Reaction Steps

1-(2,4-dichlorophenyl)-2-imidazolylethan-1-one (0.80 M) was dissolved with heating as necessary in a stirred mixture of THF (250 ml) and abs. ethanol (250 ml). After cooling to room temperature, potassium hydroxide (0.20 M) was added followed by a dropwise addition of ethyl acrylate (45.8 ml) via addition funnel over 10 min. A room temperature water bath was used to cool the exothermic reaction for the first 30 min. After stirring for 14-16 hours, the reaction was neutralized with gla. acetic acid (10 ml) and concentrated under reduced pressure. The residual dark reddish black slurry was dissolved in abs. ethanol (100 ml) and concentrated again under reduced pressure giving ethyl 5-(2,4-dichlorophenyl)-4-imidazolyl-5-oxopentanoate (2) in 108% yield. The crude material is contaminated with potassium salts and is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045519B2
Source datasetuspto-grants-2006_05
ORD IDord-41a3b9f4c33347368c218407b442f3ad
Source noteuspto-grants-2006_05