HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718166Generated: October 29, 2026
Hydrochloric Acid → HCID 136197531, compound
https://huagongshe.com/reaction/718166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclopentanecarbonyl chloride | HCID 78284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136197531 | HCID 136197531 | 38.8% |
Reaction Steps
To a suspension of semicarbazide hydrochloride (5.00 g, 44.8 mmol) in DCM (100 mL) was added triethylamine (10.00 g, 99 mmol) and the mixture was stirred at −10° C. for 30 min. Cyclopentane carbonylchloride (5.00 g, 37.7 mmol) was added at the same temp and the mixture was allowed to warm to RT over night. The solvent from the reaction mixture was completely removed and the residue stirred in MeCN (200 mL) for 1 h. The solids were collected by filtration, washed and dried. The solid was treated with sodium hydroxide (7.00 g, 175 mmol) and water (20 mL). The resulting reaction mixture was heated at 100° C. for 3 h. The reaction mixture was cooled and acidified with conc. HCl. The solids were collected, washed and dried to provide 3-cyclopentyl-1H-1,2,4-triazol-5(4H)-one (2.24 g, 38.8% yield) as white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.17 (s, 1H), 11.03 (s, 1H), 2.80 (m, 1H), 1.86 (m, 2H), 1.58 (m, 6H); MS (ESI) m/z: 154.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193719B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b67e784c2da34f468abd67166ff7692d |
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| Source note | uspto-grants-2015_11 |
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