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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644896Generated: October 30, 2026

Hydrochloric Acid → N-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamide

https://huagongshe.com/reaction/644896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethoxymethyl isothiocyanateHCID 140624—
Reactant3-(2,6-Dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazoleHCID 17862360—
SolventEthyl AcetateHCID 8857—
ProductN-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamideHCID 1786236246.7%

Reaction Steps

Potassium carbonate (0.23 g, 1.7 mmol) and methoxymethyl isothiocyanate (0.16 g, 1.5 mmol) were added to a solution of 3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole (0.47 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 white solid of N-methoxymethyl-3-(2,6-dichloro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carbothioamide (0.29 g, yield: 46.7%). mp: 95-96° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.82 (d, J=0.6 Hz, 3H), 3.41 (s, 3H), 5.10 (d, J=6.3 Hz, 2H), 5.91 (q, J=0.6 Hz, 1H), 7.68 (s, 2H), 8.80-9.20 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700786B2
Source datasetuspto-grants-2010_04
ORD IDord-abe482d8c6e3469cbe6ba9bb81d024a4
Source noteuspto-grants-2010_04