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HRID 5393作成日:2026年10月24日

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/ja/reaction/5393

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
反応物HCID 178418680HCID 178418680—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930812—

反応条件

温度0 °C

反応手順

Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (5.02 g, 20.81 mmol) is dissolved in ether (50 mL), and cooled to 0° C. Trimethylsilylmethylmagnesium chloride (42.0 mL of a 1.0M solution in ether, 42.0 mmol) is added dropwise, the reaction is stirred at 0° C. for 20 minutes, and then heated to reflux overnight. The reaction is quenched with saturated ammonium chloride, and extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (10% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-(trimethylsilylmethyl)-3-hydroxy-2-oxo-1-azacyclodecane-10-carboxylate; major isomer, m.p. 129°-130° C.; minor isomer, m.p. 175°-177° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244889
出典データセットuspto-grants-1993_09
ORD IDord-d4fb9e46ad954be7a349fa818cd8a137
出典メモuspto-grants-1993_09