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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1060806Erstellt: 26. Oktober 2026

Acetic Acid → tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylate

https://huagongshe.com/reaction/1060806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPiperidin-4-olHCID 79341—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—

Reaktionsschritte

To 1-tert-butoxycarbonyl-4-piperidone (200 g, 1.01 mol) in tetrahydrofuran (THF) (1500 ml) was added 4-hydroxypiperidine (78.1 g, 0.77 mol). The resultant slurry was stirred for 30 minutes before cooling the reaction mixture with ice/water, acetic acid (47 ml) is then added (exotherm) which caused precipitation. The slurry was allowed to warm to room temperature before the addition of sodium triacetoxyborohydride (236 g, 1.12 mol) which was washed in with THF (500 ml). The resultant slurry was stirred overnight at room temperature. To the reaction mixture was added water (2000 ml) to give a solution. The solution was then extracted with diethyl ether (3×1800 ml). The aqueous phase was basified with 10% aq NaOH (950 ml) and extracted with dichloromethane (DCM) (3×1500 ml). The combined DCM layers are dried (MgSO4), filtered and the solvent removed to give the sub-titled compound as a yellow viscous oil, (177 g, 81%; MS: (M+H) 285).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06525070B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-1aabaee4f8a14456bc000454b077cc4b
Quellennotizuspto-grants-2003_02