Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631711Generated: November 1, 2026

Potassium Carbonate → phenyl 3-ethyl-1-phenyl-1H-pyrazol-5-ylcarbamate

https://huagongshe.com/reaction/631711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-Ethyl-1-phenyl-1H-pyrazol-5-amineHCID 20297795—
SolventTetrahydrofuranHCID 8028—
Productphenyl 3-ethyl-1-phenyl-1H-pyrazol-5-ylcarbamateHCID 6687738561%

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a stirred mixture of 3-ethyl-1-phenyl-1H-pyrazol-5-amine (1.00 g, 5.34 mmol) and potassium carbonate (1.48 g, 10.68 mmol) in THF (50 mL) at −5° C., was added phenyl chloroformate (1.00 g, 6.41 mmol) dropwise. After stirring for a further 30 min at −5° C., the reaction mixture it was warmed to rt and stirred for a further 15 h. The mixture was quenched with water and extracted with dichloromethane. The combined dichloromethane layers were dried over magnesium sulfate, concentrated under reduced pressure, and dried under vacuum to afford an oil. Recrystallization from petroleum ether gave phenyl 3-ethyl-1-phenyl-1H-pyrazol-5-ylcarbamate (1.00 g, 61%) as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ 10.07 (brs, 1H), 6.74-7.59 (m, 10H), 6.30 (s, 1H), 2.60 (q, J=7.6 Hz, 2H), 1.21 (t, J=7.6 Hz, 3H); LC-MS (ESI) m/z 308 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-35f1849fa93c4a38b621518df7c7bf40
Source noteuspto-grants-2016_04