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HRID 542005생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
반응물1-Fluoro-2-iodo-4-nitrobenzeneHCID 10539733—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-[2-(2-iodo-4-nitrophenoxy)ethyl]piperidine-1-carboxylateHCID 5796263681%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871753B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-f3958cb0ed554b0182c77a915e97325f
출처 메모uspto-grants-2014_10