HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 344272Erstellt: 25. Oktober 2026
Water → 4-Hydroxy-1-(6-oxo-6-phenylhexyl)-4-tert-butoxycarbonylaminomethylpiperidine
https://huagongshe.com/reaction/344272
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-butyl N-((4-hydroxypiperidin-4-yl)methyl)carbamate | HCID 10868112 | — |
| Edukt | 1-Hexanone, 6-bromo-1-phenyl- | HCID 11242260 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Hydroxy-1-(6-oxo-6-phenylhexyl)-4-tert-butoxycarbonylaminomethylpiperidine | HCID 53842105 | 85,2% |
Reaktionsschritte
6-Bromo-1-phenyl-1-hexanone (2.9 g) and potassium carbonate (3 g) were added to a solution of 4-hydroxy-4-tert-butoxycarbonylaminomethylpiperidine (2.5 g) in dimethylformamide (40 ml), and the mixture was stirred at 60° C. for 2 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=10:1) to give 3.74 g of 4-hydroxy-1-(6-oxo-6-phenylhexyl)-4-tert-butoxycarbonylaminomethylpiperidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05864039 |
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| Quelldatensatz | uspto-grants-1999_01 |
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| ORD ID | ord-c645464eb0d84c45beb1613e171592f6 |
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| Quellennotiz | uspto-grants-1999_01 |
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