HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 482027Erstellt: 25. Oktober 2026
Dimethylformamide → 4-(Piperidin-1-yl)benzaldehyde
https://huagongshe.com/reaction/482027
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 1-Phenylpiperidine | HCID 20038 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 4-(Piperidin-1-yl)benzaldehyde | HCID 291354 | 40% |
Reaktionsschritte
To a solution of 2.3 mL (mmoles) of N,N-dimethylformamide in 10 mL of 1,2-dichloroethane was added dropwise 2.8 mL (30 mmoles) of phosphorus oxychloride at 0°C. The ice-bath was removed and the reaction mixture was stirred for 15 min. 1-Phenylpiperidine (3.2 mL, 20 mmoles) was added to the above solution portionwise and the reaction mixture was refluxed overnight. The reaction mixture was poured into ice-cold 2N sodium hydroxide solution and stirred at room temperature for 1 h. The organic layer was separated and the aqueous layer was extracted with 2×20 mL of ethyl acetate. The combined organic layer was washed with brine until pH=7, dried over anhydrous sodium sulfate and evaporated. The residue was separated on a silica gel column eluting with ethyl acetate and hexane to afford 1.5 g (40%) of the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05792783 |
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| Quelldatensatz | uspto-grants-1998_08 |
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| ORD ID | ord-8a260c01b63a431c989f5a0123438dcb |
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| Quellennotiz | uspto-grants-1998_08 |
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