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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718166Generated: October 29, 2026

Hydrochloric Acid → HCID 136197531, compound

https://huagongshe.com/reaction/718166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium HydroxideHCID 14798—
ReactantCyclopentanecarbonyl chlorideHCID 78284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 136197531HCID 13619753138.8%

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193719B2
Source datasetuspto-grants-2015_11
ORD IDord-b67e784c2da34f468abd67166ff7692d
Source noteuspto-grants-2015_11