Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921287Generated: October 30, 2026

Sodium Hydroxide → 2,2,2-Trichloroethyl 3-tert-butyl-1-P-tolyl-1H-pyrazol-5-ylcarbamate

https://huagongshe.com/reaction/1921287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
Reactant3-(tert-Butyl)-1-(p-tolyl)-1H-pyrazol-5-amine hydrochlorideHCID 11991200—
SolventEthyl AcetateHCID 8857—
Product2,2,2-Trichloroethyl 3-tert-butyl-1-P-tolyl-1H-pyrazol-5-ylcarbamateHCID 993109451.5%

Reaction Steps

To a suspension of 3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amine hydrochloride (2.5 g) in EtOAc (18 ml) was added 2.94 M aqueous NaOH (8 mL) at 0° C. under a nitrogen atmosphere, and the mixture was stirred at the same temperature for 15 min. To the reaction mixture was added 2,2,2-trichloroethyl chlorocarbonate (2.79 g), and the resulting mixture was stirred at room temperature for 6 hr. The organic layer was separated and successively washed with brine (10 mL×2), dried over MgSO4, filtered and evaporated in vacuo. The residue was triturated with IPE, and the precipitates produced were collected by filtration to give 2,2,2-trichloroethyl[3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-yl]carbamate (1.96 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173684B2
Source datasetuspto-grants-2012_05
ORD IDord-4c92c6f9db5640b7936e09c003b962f5
Source noteuspto-grants-2012_05