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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591254Generated: November 3, 2026

Hydrochloric Acid → 3-Chlorospiro-[5,6,7,8-tetrahydroquinolin-5,4'-imidazolidine]-2',5'-dione

https://huagongshe.com/reaction/1591254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium CarbonateHCID 517111—
Reactant3-Chloro-7,8-dihydroquinolin-5(6H)-oneHCID 10997654—
ReactantSodium BisulfiteHCID 23665763—
SolventFormamideHCID 713—
SolventWaterHCID 962—
Product3-Chlorospiro-[5,6,7,8-tetrahydroquinolin-5,4'-imidazolidine]-2',5'-dioneHCID 10999513—

Reaction Steps

3-Chloro-5,6,7,8-tetrahydroquinolin-5-one (125 grams, 0.689 mol) was suspended in formamide (98%, 1 L) with sodium bisulfite (73 grams, 0.7 mol). The mixture was mechanically stirred while ammonium carbonate (285 grams, 2.97 mol) was added in portions. This caused some foaming which limited the rate of addition. After the initial foaming subsided, potassium cyanide (90 grams, 1.38 mol) was added in one portion as a solid. The reaction mixture was stirred at room temperature for 3 days. The reaction was diluted with water (500 ml) and cooled in an ice water bath. The reaction pH was 9.91. 6N HCl (about 550 ml) was added dropwise to give a stable pH of 7.2. Again there was some foaming toward the end of the pH adjustment and the gases were scrubbed with a caustic trap. Water (500 ml) was added to further dilute the reaction and the mixture was granulated for 1/2 hour. The product was filtered and air dried overnight. The crude solid was broken up and slurried in acetonitrile (600 ml) for 45 minutes. The solid product was filtered, washed with acetonitrile and dried in vacuo at 40° C. Yield 134 grams (77.5%); mp 230°-3° C. NMR (DMSO, d6, 300 MHz) δ10.7 (bs, 1), 8.6 (s, 1), 8.5 (d, 1), 7.65 (d, 1), 2.9 (t, 2), 2.15 (m, 2), 1.9 (m, 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206367
Source datasetuspto-grants-1993_04
ORD IDord-b754cf765eba4f508575b8227af931ed
Source noteuspto-grants-1993_04