HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248202Erstellt: 25. Oktober 2026
Water → (1-Benzylpiperidin-4-yl)(2-methylphenyl)methanone
https://huagongshe.com/reaction/1248202
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Bromotoluene | HCID 7236 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-Benzylpiperidine-4-carbonitrile | HCID 793383 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | (1-Benzylpiperidin-4-yl)(2-methylphenyl)methanone | HCID 20530712 | — |
Reaktionsschritte
To 7 parts of magnesium is added dropwise a solution of 50 parts of 1-bromo-2-methylbenzene in 140 parts of 1,1'-oxybisethane so that the mixture is refluxing. The whole is stirred for 15 minutes at reflux. The Grignard-complex is cooled to 10° C. and there is added dropwise a solution of 30 parts of 1-(phenylmethyl)-4-piperidinecarbonitrile in 70 parts of 1,1'-oxybisethane. Upon completion, stirring is continued for 4 hours at room temperature. The reaction mixture is decomposed with a solution of 40 parts of ammonium chloride in 400 parts of water. The organic phase is separated, dried, filtered and evaporated, yielding 31 parts of (2-methylphenyl) [1-(phenylmethyl)-4-piperidinyl]methanone as an oily residue.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04522945 |
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| Quelldatensatz | uspto-grants-1985_06 |
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| ORD ID | ord-53d87a40c9db4df29be11c9aaca6526c |
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| Quellennotiz | uspto-grants-1985_06 |
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