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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648635Generated: October 30, 2026

Potassium Iodide → HCID 57115188, compound

https://huagongshe.com/reaction/648635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiethyl MalonateHCID 7761—
ReactantThionyl ChlorideHCID 24386—
ReactantSodiumHCID 5360545—
ReactantHCID 20145263HCID 20145263—
ReactantHCID 86602522HCID 86602522—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductHCID 57115188HCID 57115188—

Reaction Steps

A solution of 3.7 gm (10 m mol) of 4-[(1-(2-piperidinophenyl)-ethyl)-aminocarbonylmethyl]-benzyl chloride [m.p.: 123°-125° C.; prepared from the alcohol described in Example 25 by means of thionyl chloride in chloroform] in 35 ml of absolute ethanol was added dropwise to a solution of sodium malonic acid diethyl ester [prepared from 0.7 gm (30 m mol) of sodium in 25 ml of absolute ethanol and 4.8 gm (30 m mol) of malonic acid diethyl ester]. A catalytic amount of potassium iodide was added, and the mixture was refluxed for 16 hours. After evaporation in vacuo, the evaporation residue was adjusted neutral by means of hydrochloric acid and extracted with methylene chloride. The organic extract was dried over sodium sulfate, filtered, and evaporated in vacuo. The evaporation residue was purified by column chromatography on silica gel (toluene/acetone=6:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735959
Source datasetuspto-grants-1988_04
ORD IDord-7626ae9b2c334a888574a9918efee351
Source noteuspto-grants-1988_04