HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 642909Erstellt: 24. Oktober 2026
p-Toluenesulfonic acid → 4-(1-Benzylpiperidin-4-yl)morpholine
https://huagongshe.com/de/reaction/642909
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | 1-Benzyl-2-piperidone | HCID 5170076 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-(1-Benzylpiperidin-4-yl)morpholine | HCID 783831 | — |
Reaktionsschritte
30 mL (0.162 Mol) 1-benzylpiperidone (L) and 16.1 mL (0.185 Mol) morpholine (M) are dissolved in 407 mL tetrahydrofuran at ambient temperature. While cooling, 1.0 g (5 mmol) of p-toluenesulphonic acid and 14.6 mL glacial acetic acid are added, whereupon a jelly-like precipitate is formed. 52.19 g (0.246 Mol) sodium triacetoxyborohydride are added while cooling with ice, during which time the reaction temperature rises to 30° C. After 4 hours at 20° C., 90 mL water are added dropwise. After another 30 minutes, 280 mL of 17% potassium carbonate solution are added. The mixture is stirred intensively, while gas is observed to be given off. After separation of the phases the organic phase is dried and evaporated down. Yield: 33.0 g (78% of theory)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07696346B2 |
|---|
| Quelldatensatz | uspto-grants-2010_04 |
|---|
| ORD ID | ord-b152b6f43a19429a8b1b02915dbfe146 |
|---|
| Quellennotiz | uspto-grants-2010_04 |
|---|