HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2083670Erstellt: 26. Oktober 2026
Potassium Iodide → 2,2-Diphenyl-4-piperidin-1-ylbutanenitrile
https://huagongshe.com/reaction/2083670
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 4-Bromo-2,2-diphenylbutyronitrile | HCID 96575 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2,2-Diphenyl-4-piperidin-1-ylbutanenitrile | HCID 224577 | 86,1% |
Reaktionsschritte
To 1.96 parts of piperidine is added 1.91 parts of potassium iodide and 25 parts deionized water under a nitrogen atmosphere. The mixture is gently warmed and 1.65 parts of potassium hydroxide and 7.51 parts of 2,2-diphenyl-4-bromobutyronitrile are added. The temperature is raised to reflux and maintained thereat for 4.5 hours. After cooling to room temperature, the reaction mixture is extracted three times with 14 part portions of ethyl ether. The ether extracts are combined, and extracted four times with 25 parts by volume portions of a dilute acetic acid solution. The acid extracts are combined, neutralized to about pH 10 with 50% sodium hydroxide solution, and extracted again with ethyl ether. The ether extracts are combined, washed twice with 50 parts by volume portions of a saturated sodium chloride solution, and dried over anhydrous potassium carbonate. The solvent is removed under reduced pressure to afford, as an off-white solid, in 86.1% yield, 2,2-diphenyl-4-piperidinobutyronitrile. This compound melts at 74° - 77° C., and is represented by the following structural formula. ##STR16##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04086234 |
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| Quelldatensatz | uspto-grants-1978_04 |
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| ORD ID | ord-d64643250fdf4ac4984ab2f06ad440e5 |
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| Quellennotiz | uspto-grants-1978_04 |
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