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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21965Erstellt: 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/21965

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
PatentnummerUS05426103
Quelldatensatzuspto-grants-1995_06
ORD IDord-a31e8b575c884584a0ca2bedb89b6bf4
Quellennotizuspto-grants-1995_06