HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Propanal → tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Propanal | HCID 527 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate | HCID 21983927 | — |
| Edukt | Lithium diisopropylamine | HCID 45051747 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate | HCID 21984004 | 55,9% |
Reaktionsschritte
To a solution of tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate (0.589 g, 2.29 mmol) from Step A in tetrahydrofuran (20 mL) at −78° C. was added lithium diisopropylamine (0.650 mL, 0.974 mmol) followed by propionaldehyde (0.266 g, 0.330 mL, 4.58 mmol). After 5 min, the reaction mixture was poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 40% ethyl acetate/hexanes to afford the title compound (0.404 g). MS/EI (acetonitrile/water): m/z 216.1 (M+1−BOC) retention time=2.69 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091211B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-b89820f3efd14138aa3a6cb136df92cc |
| Quellennotiz | uspto-grants-2006_08 |