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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5407Erstellt: 23. Oktober 2026

Methanol → 3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/de/reaction/5407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium borohydrideHCID 4311764—
EduktEthyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930811—
Lösungsmitteltert-ButanolHCID 6386—
Produkt3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

The major isomer of ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate (0.68 g, 2.0 mmol) is dissolved in t-butanol (10 mL). Sodium borohydride (0.23 g, 6.0 mmol) is added and the reaction is warmed to 55° C. Methanol (2.0 mL) is added over a twenty minute period, and the reaction is kept at 55° C. for an additional 1 hour. The reaction is then partitioned between ethyl acetate and water, and the aqueous phase is extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (50% ethyl acetate/hexane) to give 3-t-butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane, MS: M+1=300.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244889
Quelldatensatzuspto-grants-1993_09
ORD IDord-429516784f194c80be8e088df5ef86d4
Quellennotizuspto-grants-1993_09