HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973673Generated: October 29, 2026
Hydrochloric Acid → HCID 67790043, compound
https://huagongshe.com/reaction/973673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Semicarbazide | HCID 5196 | — |
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Reactant | HCID 13864336 | HCID 13864336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 67790043 | HCID 67790043 | 93.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064845 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-a8ee1e53ec674d949c1afc9369001932 |
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| Source note | uspto-grants-1991_11 |
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