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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47630Generated: October 25, 2026

Water → 5-(3,5-dichloro-phenylsulphanyl)-1-ethyl-3-methyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/47630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-DichlorobenzenethiolHCID 2736096—
Reactant5-Chloro-1-ethyl-3-methyl-1H-pyrazole-4-carbaldehydeHCID 22747506—
SolventDimethylformamideHCID 6228—
Product5-(3,5-dichloro-phenylsulphanyl)-1-ethyl-3-methyl-1H-pyrazole-4-carbaldehydeHCID 2274749572.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 9.2 g of 5-chloro-1-ethyl-3-methyl-1H-pyrazole-4-carbaldehyde, 14.3 g of 3,5-dichlorothiophenol and 11.8 g of potassium carbonate in 40 ml of anhydrous N,N-dimethylformamide was stirred under nitrogen at 100° C. for 18 hours. Water (200 ml) was added and the mixture was extracted three times with 100 ml of dichloromethane. The combined extracts were dried over magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using dichloromethane/petroleum ether (bp 40-60° C.) for the elution to give 12.2 g of 5-(3,5-dichloro-phenylsulphanyl)-1-ethyl-3-methyl-1H-pyrazole-4-carbaldehyde as an orange solid. Mass spectrum (ES) m/z 356 [M+CH3CN+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699887B2
Source datasetuspto-grants-2004_03
ORD IDord-6b7b8d7a3416498d9f3bd90a8b03cd63
Source noteuspto-grants-2004_03