HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1682677Erstellt: 26. Oktober 2026
Triethylamine → t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate
https://huagongshe.com/reaction/1682677
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Tert-butyl (piperidin-4-yloxy)-acetate | HCID 10036224 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate | HCID 10066408 | 495,6% |
Reaktionsschritte
t-Butyl 4-piperidinyloxyacetate (521 mg, 2.42 mmol) and triethylamine (0.40 ml, 2.9 mmol) were dissolved in methylene chloride (20 ml) and benzyloxycarbonyl chloride (0.41 mmol, 2.9 mmol) was added. The mixture was stirred at room temperature for 74 hours. A saturated aqueous sodium hydrogencarbonate solution (50 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to give 710 mg of t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless oil (84%). Methylene chloride (30 ml) and trifluoroacetic acid (10 ml) were added to this oil (692 mg, 1.99 mmol) and the mixture was stirred at room temperature for 17 hours. Low boiling matters were distilled away from the reaction mixture under reduced pressure to give 555 mg of [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless solid (96%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05635527 |
|---|
| Quelldatensatz | uspto-grants-1997_06 |
|---|
| ORD ID | ord-f771952f11b44a4b95182564668d31c2 |
|---|
| Quellennotiz | uspto-grants-1997_06 |
|---|