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HRID 542005作成日:2026年10月24日

Sodium hydride → Tert-butyl 4-[2-(2-iodo-4-nitrophenoxy)ethyl]piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/542005

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
反応物1-Fluoro-2-iodo-4-nitrobenzeneHCID 10539733—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-[2-(2-iodo-4-nitrophenoxy)ethyl]piperidine-1-carboxylateHCID 5796263681%

反応条件

温度0 °C

反応手順

A solution of sodium hydride (0.16 g, 3.9 mmol) in tetrahydrofuran (10 mL) at 0° C. was treated with a solution of tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate (0.82 mL, 3.7 mmol) in tetrahydrofuran (5 mL) and stirred at 0° C. for 30 minutes. The reaction mixture was treated with a solution of 1-fluoro-2-iodo-4-nitrobenzene (1.0 g, 3.7 mmol) in tetrahydrofuran (5 mL) and heated at 70° C. for 16 h. The reaction mixture was concentrated, diluted with ethyl acetate, and washed with water. The aqueous layer was separated and extracted with additional ethyl acetate. The combined organic extracts were washed with brine, dried with sodium sulfate, filtered, and concentrated to a crude brown oil. Purification by flash column chromatography gave the desired product (1.4 g, 81%) as a yellow oil. LCMS for C18H251N2O5Na (M+Na)+: m/z=499.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871753B2
出典データセットuspto-grants-2014_10
ORD IDord-f3958cb0ed554b0182c77a915e97325f
出典メモuspto-grants-2014_10