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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2300164Erstellt: 27. Oktober 2026

Tert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate → tert-Butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/2300164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 22744533—
EduktHCID 178418361HCID 178418361—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 2274454989,1%

Reaktionsschritte

6.47 g of tert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate was dissolved in 100 ml tetrahydrofuran, 1.3 g palladium carbon was added thereto, and the mixture was stirred overnight in a hydrogen atmosphere. The catalyst was filtered off from the reaction solution, 1.3 g of palladium carbon was added thereto, and the solution was stirred overnight in a hydrogen atmosphere. The catalyst was filtered off from the reaction solution, 2.6 g of palladium carbon was added thereto, and the solution was stirred overnight in a hydrogen atmosphere at 4.2 atmospheric pressure. The catalyst was filtered off from the reaction solution, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give 4.27 g of tert-butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06498159B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-9568fe80ede14ae1be604142cfec6a1f
Quellennotizuspto-grants-2002_12