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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644894Generated: October 30, 2026

Hydrochloric Acid → HCID 17862379, compound

https://huagongshe.com/reaction/644894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl isocyanateHCID 8022—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 17862446HCID 17862446—
SolventEthyl AcetateHCID 8857—
ProductHCID 17862379HCID 1786237954.3%

Reaction Steps

Potassium carbonate (0.25 g, 1.8 mmol) and ethyl isocyanate (0.11 g, 1.5 mmol) were added to a solution of 5-(4-chlorophenyl)-3-(2,6-dichloro-4-trifluoromethylphenyloxy)pyrazole (0.61 g, 1.5 mmol) in ethyl acetate (10 ml), and the mixture was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was poured into 2N hydrochloric acid and extracted with ethyl acetate (10 ml×3). An organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered to remove a desiccant, and the solvent was distilled off from the filtrate under reduced pressure. The resultant crude product was purified with a silica gel column (ethyl acetate/hexane=1/7), to give a white solid of N-ethyl-5-(4-chlorophenyl)-3-(2,6-dichloro-4-trifluoromethylphenyloxy)pyrazole-1-carboxamide (0.39 g, yield: 54.3%). mp: 88-89° C.; 1H-NMR (CDCl3, TMS, ppm): δ 1.17 (t, J=7.3 Hz, 3H), 3.30 (dq, J=6.1 and 7.3 Hz, 2H), 5.96 (s, 1H), 6.65-6.85 (m, 1H), 7.30-7.50 (m, 4H), 7.70 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-7e969dd272d446e99b4aa46509eace3f
Source noteuspto-grants-2010_04