Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Hydroxypiperidine | HCID 20935 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178478979 | HCID 178478979 | — |
| Katalysator | Manganese dioxide | HCID 14801 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Phenylpiperidin-1-ol | HCID 15270572 | 38% |
Reaktionsschritte
Activated MnO2 (1.29 g, 14.8 mmol) was added to a solution of N-hydroxypiperidine (0.50 g, 4.95 mmol) in dichloromethane (25 mL) at 0° C. and the mixture was stirred for 1 h. The reaction mixture was filtered through a pad of Celite™ and Na2SO4. The filtrate was added dropwise to a solution of phenylmagnesium chloride (2.0 M in tetrahydrofuran, 4.95 mL, 9.90 mmol) at −10° C. The reaction mixture was stirred at 0° C. for 0.5 h and then saturated aqueous ammonium chloride solution (25 mL) and dichloromethane (25 mL) were added. The aqueous phase was separated and extracted with dichloromethane (2×30 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The crude product was subjected to flash chromatography on SiO2 eluting with 30% diethyl ether in hexanes to give the title compound (0.330 g, 38%) as a white crystalline solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08053432B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-3113904f2c3548cb869c6591f2d93bd0 |
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| Quellennotiz | uspto-grants-2011_11 |
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