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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2206362Erstellt: 26. Oktober 2026

2-(Dimethylamino)ethanol → 2-(3-bromo-5-nitrophenoxy)-N,N-dimethylethanamine

https://huagongshe.com/reaction/2206362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Dimethylamino)ethanolHCID 7902—
EduktPotassium HydroxideHCID 14797—
Edukt1-Bromo-3,5-dinitrobenzeneHCID 44534—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(3-bromo-5-nitrophenoxy)-N,N-dimethylethanamineHCID 5931399357,2%

Reaktionsschritte

1-Bromo-3,5-dinitrobenzene (1 g, 4.1 mmol), 2-(dimethylamino)ethanol (0.54 g, 6.1 mmol), potassium hydroxide (0.45 g, 8.1 mmol), and water (0.5 mL) in DMF (5 mL) were heated at 80° C. After 20 hours, the reaction mixture was diluted with cold water and extracted with dichloromethane (2×100 mL). The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel chromatography (stepwise gradient, 2% ethyl acetate in hexanes to ethyl acetate) to give 2-(3-bromo-5-nitrophenoxy)-N,N-dimethylethanamine (669 mg, 57.2% yield) as a brown oil. HPLC: Rt=1.04 min. (PHENOMENEX® Luna 5 micron C18 4.6×30 mm, 10-90% aqueous methanol containing 0.1% TFA, 2 min. gradient, flow rate=5 mL/min., detection at 254 nm). MS (ES): m/z=290.93 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09371328B2
Quelldatensatzuspto-grants-2016_06
ORD IDord-ef9a9b6f39914e55a30293fae4e90ee4
Quellennotizuspto-grants-2016_06