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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55986Generated: October 30, 2026

Water → N-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]phthalimide

https://huagongshe.com/reaction/55986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
ReactantN-[2-(3,5-dichloropyridin-2-yl)-2-(hydroxyimino)ethyl]phthalimideHCID 136987064—
SolventDimethylformamideHCID 6228—
ProductN-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]phthalimideHCID 11807153979.2%

Reaction Steps

To 265 mg of N-[2-(3,5-dichloropyridin-2-yl)-2-(hydroxyimino)ethyl]phthalimide in 2 ml of N,N-dimethylformamide, 310 mg of potassium carbonate and 387 mg of 1-iodopropane were added, and the mixture was stirred at room temperature for 18 hours. After completion of the reaction, the reaction mixture was mixed with 30 ml of water and extracted with ethyl acetate (50 ml×1), the resulting organic layer was washed with water (50 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 15:85 to 25:75) as the eluent to obtain 235 mg of the desired product as a yellow resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434684B2
Source datasetuspto-grants-2016_09
ORD IDord-0d347aef2e154005be744f8d1f13d25a
Source noteuspto-grants-2016_09