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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1668460Erstellt: 26. Oktober 2026

Sodium Dithionite → 4-Bromo-2-(2,2-dimethoxyethyl)aniline

https://huagongshe.com/reaction/1668460

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium DithioniteHCID 24489—
EduktSodium BicarbonateHCID 516892—
Edukt4-Bromo-2-(2,2-dimethoxyethyl)-1-nitrobenzeneHCID 59004646—
LösungsmittelEthanolHCID 702—
Produkt4-Bromo-2-(2,2-dimethoxyethyl)anilineHCID 5900460947,5%

Reaktionsschritte

Compound 66 (75 mg, 0.259 mmol) was dissolved in anhydrous ethanol (10 mL) in a dry argon purged flask fitted with a magnetic stir bar and condenser. Sodium dithionite (158.8 mg, 0.776 mmol) and sodium bicarbonate (130.6 mg, 1.554 mmol) are added to the flask and mixture heated to reflux for 24 hours. After cooling to room temperature, the reaction was quenched by the addition of H2O (10 mL) and the ethanol removed under reduced pressure. The resulting aqueous layer was transferred to a separatory funnel and extracted with ethyl acetate (three times). The combined organic layers were washed with brine, dried over sodium sulphate, filtered, concentrated and the residue purified via chromatography on silica gel (methanol:CH2Cl2, 2:98) to yield a brown oil, 67 (32 mg, 47.5%). 1H NMR (CDCl3) δ 2.83 (d, 2H, J=5.3 Hz), 3.38 (s, 6H), 4.48 (t, 1H, J=5.3 Hz), 6.61 (d, 1H, J=8.2 Hz), 7.13 (d, 1H, J=2.2 Hz), 7.15-7.17 (m, 1H); ESI-MS (m/z, %): 198/200 (M+−2MeO, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07989447B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-945e3c0d470244abbf24c862108876e9
Quellennotizuspto-grants-2011_08