Sodium hydride → HCID 10906020, Verbindung

A solution of diallyl 2-methylmalonate (396 mg, 2 mmol) in tetrahydrofuran (2 ml) was added dropwise to a suspension of sodium hydride (80 mg, 2 mmol) in tetrahydrofuran (5 ml) under an argon stream at 0° C., and the solution mixture was stirred for 5 min and admixed with cuprous bromide dimethylsulfide complex (411 mg, 2 mmol), followed by stirring for 30 min at the same temperature, addition of a solution of (3R,4S)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-phenylthio-2-azetidinone (338 mg, 1 mmole) in tetrahydrofuran (3 ml) and stirring for 1 hour. The reaction solution was admixed with aqueous saturated ammonium chloride solution and extracted with ethyl acetate. The ethyl acetate layer was dried over magnesium sulfate and concentrated under reduced pressure, and the residue was purified by column chromatography (10 g of silica gel; a 8/1 mixture of n-hexane/ethyl acetate) to give 392 mg (92%) of the subject compound in the form of colorless crystals.

1. stirringstirring for 1 hour
2. extractionextracted with ethyl acetate
3. dry with materialThe ethyl acetate layer was dried over magnesium sulfate
4. concentrationconcentrated under reduced pressure
5. customthe residue was purified by column chromatography (10 g of silica gel
6. additiona 8/1 mixture of n-hexane/ethyl acetate)

ORD-Eintrag

ord-9407208f648249568bb96afc2f20183a

Quelldatensatz

uspto-grants-2005_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06867297B1