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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718195Generated: October 30, 2026

Semicarbazide → HCID 136641697, compound

https://huagongshe.com/reaction/718195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSemicarbazideHCID 5196—
ReactantDimethylformamideHCID 6228—
ReactantSemicarbazide hydrochlorideHCID 11236—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Benzyloxy)-2,2-dimethylpropanoic acidHCID 13478288—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 136641697HCID 13664169748%

Reaction Steps

3-(Benzyloxy)-2,2-dimethylpropanoic acid (1.00 g, 4.80 mmol) was dissolved in DCM (10 mL) at RT. Oxalyl chloride (0.70 mL, 8.00 mmol) and DMF (0.10 mL, 1.29 mmol) were added sequentially and the reaction mixture was stirred at RT for 2 h. In a separate flask, semicarbazide hydrochloride (0.8 g, 7.24 mmol) and NaOH (0.80 g, 20.0 mmol) were dissolved in a solution of dioxane (2.0 mL) and water (10.0 mL). The solution of the acid chloride was added in one portion to the solution of the semicarbazide and the reaction mixture was stirred at RT for 12 h. 2 M NaOH (aq.) (28.0 mL, 56.0 mmol) was then added and the reaction mixture was stirred at 100° C. for 2 h, allowed to cool to RT, and neutralized by the addition of ¾ sat. NH4Cl (aq.) (75 mL). The resultant homogenous solution was sonicated for 12 h and the resultant precipitated solids were collected by filtration and dried in vacuo to afford 3-(1-(benzyloxy)-2-methylpropan-2-yl)-1H-1,2,4-triazol-5(4H)-one (0.57 g, 48.0%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.22 (s, 1H), 11.09 (s, 1H), 7.34-7.23 (m, 5H), 4.44 (s, 2H), 3.39 (s, 2H), 1.16 (s, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193719B2
Source datasetuspto-grants-2015_11
ORD IDord-b8b710ae593e462e8327a0b6f622729f
Source noteuspto-grants-2015_11