HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648635Generated: October 30, 2026
Potassium Iodide → HCID 57115188, compound
https://huagongshe.com/reaction/648635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20145263 | HCID 20145263 | — |
| Reactant | HCID 86602522 | HCID 86602522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 57115188 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735959 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-7626ae9b2c334a888574a9918efee351 |
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| Source note | uspto-grants-1988_04 |
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