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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21978Erstellt: 24. Oktober 2026

tert-Butyl Dimethylphosphonoacetate → Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/de/reaction/21978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl DimethylphosphonoacetateHCID 4564495—
EduktEthyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylateHCID 54383214—

Reaktionsschritte

Potassium hexamethyldisilylamide (40.5 mL of a 0.58M solution in toluene, 23.5 mmol) is added to THF (60 mL), and then cooled to 0° C. t-Butyl dimethylphosphonoacetate (4.6 mL, 23.5 mmol) is added dropwise, and the reaction is warned to room temperature and stirred for 25 minutes. Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (2.83 g, 11.74 mmol) is added in THF (15 mL), and the reaction is stirred at room temperature for 2.5 hours. The reaction is quenched with saturated ammonium chloride, and then extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05426103
Quelldatensatzuspto-grants-1995_06
ORD IDord-abd37e9569de41e18c1a8ba201ccfeea
Quellennotizuspto-grants-1995_06