Reaktion #560623

Reaktionsgleichung

(S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate

isopropylmagnesium chloride

benzylmagnesium chloride

→

(S)-tert-butyl 3-oxo-4-phenylbutan-2-ylcarbamate

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter a clear solution was obtained
2. 2
   SonstigeThe reaction mixture was quenched with NH4Cl solution
3. 3
   Extraktionextracted with EtOAc (10 mL×2)
4. 4
   WaschenThe combined organic layers were washed with water, brine
5. 5
   Trocknendried over sodium sulfate
6. 6
   Filtrationbefore being filtered
7. 7
   Einengenconcentrated

Vorschrift

A solution of (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate (1.16 g, 5 mmol) in THF (10 mL) was cooled to −15° C. and slowly charged with isopropylmagnesium chloride (2.0M, 2.37 mL, 0.95 eq). After a clear solution was obtained, benzylmagnesium chloride (1.0M, 4.99 mL, 1.0 eq) was added dropwise with stirring at rt overnight. The reaction mixture was quenched with NH4Cl solution and extracted with EtOAc (10 mL×2). The combined organic layers were washed with water, brine, dried over sodium sulfate before being filtered, concentrated to give a white solid as (S)-tert-butyl 3-oxo-4-phenylbutan-2-ylcarbamate. Mass Spectrum (ESI) m/e=264 (M+1).

Quelle