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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8759Erstellt: 24. Oktober 2026

tert-Butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylate → tert-Butyl 4-oxo-3-(1-oxoprop-1-yl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/de/reaction/8759

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylateHCID 73857865—
KatalysatorDirhodium tetraacetateHCID 152122—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl 4-oxo-3-(1-oxoprop-1-yl)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 2198389240,4%

Reaktionsschritte

A solution of rhodium acetate dimer (0.002 g, 0.005 mmol) in dichloromethane (27 mL) was heated to 81° C. A solution of tert-butyl 4-methoxy-4-(2-diazo-1,3-dioxopent-1-yl)piperidine-1-carboxylate (0.092 g, 0.270 mmol) from Step D in dichloromethane (7 mL) was added slowly dropwise over 12 min. The reaction mixture was refluxed for 45 min then poured into IN hydrochloric acid, and extracted three times with dichloromethane. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 10% ethyl acetate/dichloromethane to afford the title compound (0.034 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091211B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-877888e2a7554dd4b0bc69673d1bcb3a
Quellennotizuspto-grants-2006_08