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HRID 5407作成日:2026年10月23日

Methanol → 3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/ja/reaction/5407

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium borohydrideHCID 4311764—
反応物Ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930811—
溶媒tert-ButanolHCID 6386—
生成物3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—

反応条件

温度55 °C

反応手順

The major isomer of ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate (0.68 g, 2.0 mmol) is dissolved in t-butanol (10 mL). Sodium borohydride (0.23 g, 6.0 mmol) is added and the reaction is warmed to 55° C. Methanol (2.0 mL) is added over a twenty minute period, and the reaction is kept at 55° C. for an additional 1 hour. The reaction is then partitioned between ethyl acetate and water, and the aqueous phase is extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (50% ethyl acetate/hexane) to give 3-t-butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane, MS: M+1=300.

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-429516784f194c80be8e088df5ef86d4
出典メモuspto-grants-1993_09