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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277519Generated: November 2, 2026

Ammonia → HCID 23454279, compound

https://huagongshe.com/reaction/1277519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantHCID 23454277HCID 23454277—
ReactantHCID 23454280HCID 23454280—
SolventChloroformHCID 6212—
ProductHCID 23454279HCID 2345427983.2%

Reaction Steps

110 g (0.5 mol) of 8-chloro-5,6,7,8-tetrahydro-2-quinolone hydrochloride are heated with 500 ml of water to about 90° C. with agitation, thus obtaining after a short time a transparent solution which is then neutralized with 75 ml of concentrated ammonia. After cooling of the solution, 105 g of 8-hydroxy-5,6,7,8-tetrahydro-2-quinolone trihydrate areisolated having a melting point of 192° C., which correspond to a yield of 85.7% of theory. 105 g (0.48 mol) of trihydrate are heated with 2liters of chloroform while stirring, the hydration water is removed in the form of an azeotropic mixture, and the chloroform phase of the distillate is recycled to the flask. After this operation is complete, 350 g of manganese dioxide (precipitated in an active form) are added to the chloroform solution in portions and in such a manner that the reaction temperature does not exceed 40° C. Intense agitation is continued at this temperature for 3 hours. Subsequently, the batch is separated fromthe manganese dioxide, the chloroform is distilled off, and 65 g of light brown 8-oxo-5,6,7,8-tetrahydro-2-quinolone, corresponding to a yield of 83% of theory, are isolated, which after recrystallization from cyclohexanone has a melting point of 253° C. in a closed vial.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277606
Source datasetuspto-grants-1981_07
ORD IDord-c8f089e7f6504a9fbaecd1d94fc89338
Source noteuspto-grants-1981_07