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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukttert-butyl N-((4-hydroxypiperidin-4-yl)methyl)carbamateHCID 10868112—
Edukt1-Hexanone, 6-bromo-1-phenyl-HCID 11242260—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Hydroxy-1-(6-oxo-6-phenylhexyl)-4-tert-butoxycarbonylaminomethylpiperidineHCID 5384210585,2%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05864039
Quelldatensatzuspto-grants-1999_01
ORD IDord-c645464eb0d84c45beb1613e171592f6
Quellennotizuspto-grants-1999_01