Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644889Generated: October 30, 2026

Hydrochloric Acid → HCID 59263964, compound

https://huagongshe.com/reaction/644889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl isocyanateHCID 8022—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 17862342HCID 17862342—
SolventEthyl AcetateHCID 8857—
ProductHCID 59263964HCID 5926396488.2%

Reaction Steps

Potassium carbonate (0.23 g, 1.7 mmol) and ethyl isocyanate (0.11 g, 1.5 mmol) were added to a solution of 5-cyclopropyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)pyrazole (0.51 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=1/10), to give a colorless viscous substance of N-ethyl-5-cyclopropyl-3-(2,6-dichloro-4-trifluoromethylpheyloxy)pyrazole-1-carboxamide (0.54 g, yield: 88.2%). 1H-NMR (CDCl3, TMS, ppm): δ 0.70 (m, 2H), 1.07 (m, 2H), 1.20 (t, J=7.3 Hz, 3H), 2.81 (m, 1H), 3.36 (dq, J=6.0 and 7.3 Hz, 2H), 5.45 (s, 1H), 6.60-6.85 (m, 1H), 7.66 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-cc9f4f15d9584cb281f752e800a9baa9
Source noteuspto-grants-2010_04