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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604439Generated: October 29, 2026

Diethyl Ether → 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-dimethoxymethyl-4-trifluoromethylthiopyrazole

https://huagongshe.com/reaction/1604439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTrimethyl orthoformateHCID 9005—
Reactant3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-formyl-4-trifluoromethylthiopyrazoleHCID 11812098—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventMethanolHCID 887—
Product3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-dimethoxymethyl-4-trifluoromethylthiopyrazoleHCID 984799376.2%

Reaction Steps

The product of Example 3(2.0 g, 0.005 mol) was combined with trimethylorthoformate (10 ml, 0.09 mol) and para-toluenesulfonic acid monohydrate (50 mg, catalytic) in anhydrous methanol. The mixture was refluxed for 72 hours, cooled to room temperature, poured into diethyl ether, washed with a 1:1 mixture of 10% aqueous sodium hydroxide solution and concentrated aqueous sodium chloride solution (100 ml), water (100 ml) and saturated aqueous sodium chloride solution (100 ml). The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo to leave an oil that was purified by silica gel chromatography using a 3:1 hexane:dichloromethane solvent mixture. This provided the title compound as a white solid (1.83 g), m.p. about 93° C. Also prepared by this method: Compound 18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994386
Source datasetuspto-grants-1999_11
ORD IDord-cf790ffaade141a5a6fabf3882853d81
Source noteuspto-grants-1999_11