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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5393Erstellt: 24. Oktober 2026

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/de/reaction/5393

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
EduktHCID 178418680HCID 178418680—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930812—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (5.02 g, 20.81 mmol) is dissolved in ether (50 mL), and cooled to 0° C. Trimethylsilylmethylmagnesium chloride (42.0 mL of a 1.0M solution in ether, 42.0 mmol) is added dropwise, the reaction is stirred at 0° C. for 20 minutes, and then heated to reflux overnight. The reaction is quenched with saturated ammonium chloride, and extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate; major isomer, m.p. 129°-130° C.; minor isomer, m.p. 175°-177° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244889
Quelldatensatzuspto-grants-1993_09
ORD IDord-d4fb9e46ad954be7a349fa818cd8a137
Quellennotizuspto-grants-1993_09