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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903612Generated: October 26, 2026

Hydrochloric Acid → 2H,5H-Spiro[imidazolidine-4,5'-indeno[1,2-b]pyridine]-2,5-dione

https://huagongshe.com/reaction/1903612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPotassium CyanideHCID 9032—
Reactant5H-Indeno(1,2-b)pyridin-5-oneHCID 77489—
ReactantAmmonium CarbonateHCID 517111—
Product2H,5H-Spiro[imidazolidine-4,5'-indeno[1,2-b]pyridine]-2,5-dioneHCID 13491384—

Reaction Steps

4-Aza-9-fluorenone (Aldrich Chemical Co.), (2.4 g, 13.3 mmol), KCN (2.0 g, 30.7 mmol) and ammonium carbonate (5.0 g) in 80% ethanol (50 cc) were placed in a thick walled glass pressure reactor. The mixture was heated at 110°-115° C. for 12 hours. The reaction vessel was cooled and ice water (200 mL) was added to the reaction mixture. Dilute hydrochloric acid was added until pH was approximately 8 and the solid was collected by filtration. The collected solid was dissolved in 5% sodium hydroxide and treated with activated charcoal and filtered through a Celite (diatomaceous earth filter aid) pad. The solution was adjusted to pH 7-8 by the addition of 1 N hydrochloric acid. The resulting precipitate was collected on a filter, washed with cold water and dried to yield a sample of dl-Spiro-(4-aza-fluorene-9,4'-imidazolidine)-2',5'-dione (1.4 g) having a melting point of 311°-312° C. with dec., m/e+ . 251 for C14H9N3O2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436745
Source datasetuspto-grants-1984_03
ORD IDord-f7732923cbb04115a7b5543aff4f4f88
Source noteuspto-grants-1984_03