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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256145Generated: October 30, 2026

Imidazole → [5-(1H-Imidazol-1-yl)-1-oxo-2,3-dihydro-1H-inden-2-yl]acetic acid

https://huagongshe.com/reaction/256145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10443021HCID 10443021—
SolventPyridineHCID 1049—
Product[5-(1H-Imidazol-1-yl)-1-oxo-2,3-dihydro-1H-inden-2-yl]acetic acidHCID 1365605039.4%

Reaction Steps

A mixture of 3.3 g of 5-fluoro-2,3-dihydro-1-oxo-1H-indene-2-acetic acid [prepared by following the procedure of G. Cignarella, M. Loriga, G. A. Pinna, M. A. Pirisi, P. Schaitti, and D. Selva, Il Farmaco, Ed. Sci. 37(2), 133-40 (1981)], 2.2 g of anhydrous K2CO3, 1.65 g of imidazole, and 0.15 g of CuO in 15 ml of pyridine is heated to reflux for 24 hours. The reaction mixture is filtered, the filtrate is diluted with water, and the pH of the solution is adjusted to 5. The solid is filtered, washed with water, and crystallized from ethanol to yield 1.6 g of the product, 2,3-dihydro-5-(1H-imidazol -1-yl)-1-oxo-1H-indene-2 acetic acid, mp 224°-226° dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04701453
Source datasetuspto-grants-1987_10
ORD IDord-3e0b3e6e5125470887c67e547a6fb303
Source noteuspto-grants-1987_10