HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1058779Erstellt: 25. Oktober 2026
Hydrochloric Acid → (+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidine
https://huagongshe.com/reaction/1058779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 1,4-Difluorobenzene | HCID 10892 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Phenyl-piperidin-4-yl-methanol | HCID 339086 | — |
| Edukt | Potassium Benzoate | HCID 23661960 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (+)-4-[(4-Fluorophenoxy)phenyl]methyl-piperidine | HCID 18669358 | 54% |
Reaktionsschritte
The alcohol prepared above (2.7 g, 9.3 mmol) dissolved in DMSO (25 mL) was added over an NaH (60%, 0.6 g) suspension in DMSO (5 mL). Potassium benzoate (1.53 g, 9.63 mmol) and 1,4-difluorobenzene (1.3 mL, 11.9 mmol) were added and the mixture was heated (70-75° C.) until the starting substance disappeared. The reaction mixture was poured into water and saturated aqueous NaCl solution, and extracted with ether. The oil obtained was refluxed with a mixture of methanol (40 mL) and an aqueous hydrochloric acid (40 mL) solution for 1 h. Isolation of the product using the customary methodology provided (+)-4-[(4-fluorophenoxy)phenyl]methyl-piperidine as an oil in a 54% yield. Treatment of 0.5 g (1.75 mmol) of this oil with D-dibenzoyltartaric acid in ethanol (96%, 30 mL) provided a precipitate which was filtered (m.p.=198-199° C.). The aminoether was released yielding a white solid with a 96% ee, m.p.=102-104° C., and [α]546+15, c=0.105, CHCl3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06518284B2 |
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| Quelldatensatz | uspto-grants-2003_02 |
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| ORD ID | ord-49fa5571b1d440ebad6f0f55ec530ec2 |
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| Quellennotiz | uspto-grants-2003_02 |
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