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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350887Generated: October 25, 2026

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

https://huagongshe.com/reaction/350887

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+CH3CH+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183296B2
Source datasetuspto-grants-2007_02
ORD IDord-95b2ae22c5c745bcbcd022c45c8414b3
Source noteuspto-grants-2007_02