Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499993Generated: October 29, 2026

Tert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate → 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole

https://huagongshe.com/reaction/499993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylateHCID 57548571—
SolventEthyl AcetateHCID 8857—
Product3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazoleHCID 1786242889%

Reaction Steps

To an ethyl acetate (100 mL) solution of tert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate (49.7 g, 126 mmol) was added 3 mol/L of HCL (40 mL), and the mixture was refluxed under heating for 2 hours. After completion of the reaction, the reaction mixture was consecutively washed with water and a 1 mol/L sodium hydroxide aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off to give a white solid of 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (33.0 g, yield: 89.0%). Melting point: 116˜117° C., 1H-NMR (CDCl3, TMS, ppm): δ2.24 (s, 3H), 5.69 (s, 1H), 7.36 (dd, J=1.8 Hz, JHF=9.4 Hz, 1H), 7.50-7.60 (m, 1H), 9.00-9.30 (brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767827B2
Source datasetuspto-grants-2010_08
ORD IDord-342196a38a7e457c9688c647f4c23adb
Source noteuspto-grants-2010_08