Reaktion #1345
ord-bcfe7e4ce5914fd798eabd94aed3d84f
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe resulting mixture was cooled in an ice bath
- 2SonstigeThe reaction mixture was then quenched with water (100 mL) and tetrahydrofuran
- 3Sonstigewas removed under reduced pressure
- 4ExtraktionThe aqueous phase was extracted with ethyl acetate (3×250 mL)
- 5TrocknenThe combined organic fractions was dried (sodium sulfate)
- 6Filtrationfiltered
- 7Einengenconcentrated in vacuo
- 8SonstigeThe residue was purified by flash chromatography on silica gel (grade 9385, Merck, 230-400 mesh, 60 Å)
- 9workup.ADDITIONa mixture of hexane and ethyl acetate (9:1 and 8:2
Vorschrift
To a suspension of sodium hydride (55 g, 60% dispersion in oil) in tetrahydrofuran (1L) under a nitrogen atmosphere was added a solution of 2,2-dimethyl-[1,3]dioxolane-4-methanol (XV, 102.4 g) in tetrahydrofuran (250 mL) over 15 min at room temperature. The resulting mixture was cooled in an ice bath and a solution of ethyl 4-chloroacetoacetate (VIII, 102.9 g) in tetrahydrofuran (250 mL) was added dropwise over a period of 1 h. The reaction mixture was stirred at room temperature for 20 h. The reaction mixture was then quenched with water (100 mL) and tetrahydrofuran was removed under reduced pressure. The aqueous phase was extracted with ethyl acetate (3×250 mL). The combined organic fractions was dried (sodium sulfate), filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (grade 9385, Merck, 230-400 mesh, 60 Å) using a mixture of hexane and ethyl acetate (9:1 and 8:2; 2L each) as eluent, thereby affording the title compound (XVI, 81.6 g). IR (neat, cm-1): 1736. (Alker, D. J. Med. Chem. 1991, 34, 19).