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HRID 21978作成日:2026年10月26日

tert-Butyl Dimethylphosphonoacetate → Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/reaction/21978

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl DimethylphosphonoacetateHCID 4564495—
反応物Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylateHCID 54383214—

反応手順

Potassium hexamethyldisilylamide (40.5 mL of a 0.58M solution in toluene, 23.5 mmol) is added to THF (60 mL), and then cooled to 0° C. t-Butyl dimethylphosphonoacetate (4.6 mL, 23.5 mmol) is added dropwise, and the reaction is warned to room temperature and stirred for 25 minutes. Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (2.83 g, 11.74 mmol) is added in THF (15 mL), and the reaction is stirred at room temperature for 2.5 hours. The reaction is quenched with saturated ammonium chloride, and then extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426103
出典データセットuspto-grants-1995_06
ORD IDord-abd37e9569de41e18c1a8ba201ccfeea
出典メモuspto-grants-1995_06