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HRID 1249作成日:2026年10月23日

Solketal → 4-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-oxo-butyric acid ethyl ester

https://huagongshe.com/ja/reaction/1249

反応式

関与物質

役割名称HCID仕込み量
反応物SolketalHCID 7528—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 4-chloroacetoacetateHCID 69484—
溶媒TetrahydrofuranHCID 8028—
生成物4-(2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-oxo-butyric acid ethyl esterHCID 1987128850.1%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723618
出典データセットuspto-grants-1998_03
ORD IDord-bcfe7e4ce5914fd798eabd94aed3d84f
出典メモuspto-grants-1998_03