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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274861Generated: November 1, 2026

Hydrochloric Acid → HCID 67790043, compound

https://huagongshe.com/reaction/274861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSemicarbazideHCID 5196—
ReactantEthyl isocyanateHCID 8022—
Reactant4-ChlorobenzohydrazideHCID 10816—
ReactantHCID 13864336HCID 13864336—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 67790043HCID 6779004393.5%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a suspension of 4-chlorobenzhydrazide (98.5 g, 0.05 mole) in tetrahydrofuran (100 ml) at room temperature ethylisocyanate (4.2 g, 0.05 mole) was added slowly with magnetic stirring. The reaction was slightly exothermic and the reaction mixture turned to a thick paste. Stirring was continued an additional 30 min after which the solid was collected by suction-filtration and washed with a small amount of tetrahydrofuran and dried to provide 11.6 g (96.6% yield), of 1-(4-chlorobenzoyl)-4-ethyl semicarbazide as a white solid., m.p.=242°-243° C. The above semicarbazide (10 g, 0.0414 mole) was dissolved in 1N sodium hydroxide solution (100 ml) and was refluxed with stirring for 16 hr. The solution was cooled down to about 10° C. by an ice bath and was neutralized by conc. hydrogen chloride until pH 2. The resultant white solid was collected by suction-filtration and washed with water to give 8.65 g (93.5% yield) of 3-(4-chlorophenyl)-4-ethyl-1,2,4-triazolin-5-one as a white solid. m.p.=190°-197° C. A proton NMR spectrum was consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391561
Source datasetuspto-grants-1995_02
ORD IDord-ecf953b60fa643bc95c033d5e2df0db9
Source noteuspto-grants-1995_02