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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 987920Erstellt: 24. Oktober 2026

Cerium(III) chloride → 4-Benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/de/reaction/987920

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCerium(III) chlorideHCID 24636—
EduktSodium borohydrideHCID 4311764—
Edukt4-Benzyl-5-(2-tert-butylcarbamoyl-4-oxo-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 69854080—
LösungsmittelMethanolHCID 887—
Produkt4-Benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6985478277,8%

Reaktionsschritte

A solution of 4-benzyl-5-(2-tert-butylcarbamoyl-4-oxo-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.1 g, 2.2 mmol) in dry methanol (20 ml) was stirred at room temperature under nitrogen during the addition of cerium chloride (1.8 g, 4.84 mmol). The resulting mixture was stirred at room temperature for 30 minutes, then cooled to −78° C. and treated with sodium borohydride (183 mg, 4.84 mmol). The resulting suspension was allowed to warm to 0° C. over 90 min, then partitioned between ethyl acetate and a mixture of saturated aqueous ammonium chloride solution and brine. The two layers were separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic layers were dried (anhydrous magnesium sulfate) and concentrated in vacuo. Purification by flash chromatography on silica gel (ethyl acetate/hexane: 1/1 to 2/1) provided 4-benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (860 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06632826B1
Quelldatensatzuspto-grants-2003_10
ORD IDord-8d2d03d10be3438e94fcce368d028557
Quellennotizuspto-grants-2003_10