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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542005Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
Edukt1-Fluoro-2-iodo-4-nitrobenzeneHCID 10539733—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 4-[2-(2-iodo-4-nitrophenoxy)ethyl]piperidine-1-carboxylateHCID 5796263681%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871753B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-f3958cb0ed554b0182c77a915e97325f
Quellennotizuspto-grants-2014_10