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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13104Erstellt: 24. Oktober 2026

Ethyl Acetate → (S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamate

https://huagongshe.com/de/reaction/13104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAmmonium ChlorideHCID 25517—
Edukt(S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamateHCID 9992774—
EduktHCID 178418255HCID 178418255—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamateHCID 59339674—

Reaktionsschritte

In a 50 mL round-bottomed flask was (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamate (91d, 250 mg, 0.96 mmol) dissolved in THF (9.6 ml). Phenylmagnesium bromide (2.88 ml, 2.88 mmol) 1.0 M in THF was added. The reaction was stirred at r.t. for 5 h. The reaction was poured into a mixture of saturated ammonium chloride and ethyl acetate. The mixture was shaken and the layers separated. The water layer was washed twice with ethyl acetate. The combined organic layers were washed once with a small portion of water and dried over sodium sulphate. The solvent was evaporated and the crude product was purified by flash chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728030B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1ba14a93921b47a5b43504fa8549e008
Quellennotizuspto-grants-2010_06