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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 625385Erstellt: 24. Oktober 2026

Potassium Iodide → 3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acid

https://huagongshe.com/de/reaction/625385

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt1,2-Ethanediamine, N1,N1-diethyl-N2-methyl-HCID 66034—
Edukt3-(Bromomethyl)benzoic acidHCID 245650—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acidHCID 6658683948,8%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Into a 1000-mL round bottom flask, was placed a solution of N1,N1-diethyl-N2-methylethane-1,2-diamine (9.1 g, 63.00 mmol, 1.50 equiv, 90%) in N,N-dimethylformamide (500 mL), 3-(bromomethyl)benzoic acid (10 g, 46.51 mmol, 1.00 equiv), potassium carbonate (7.8 g, 56.12 mmol, 1.20 equiv), and potassium iodide (1.55 g, 9.34 mmol, 0.20 equiv). The resulting solution was stirred for 2 h at 90° C. in an oil bath. The solids were filtered out. The resulting mixture was concentrated under vacuum. The crude product (10 g) was purified by reverse phase HPLC eluting with 0.05% TFA in a water/CH3CN gradient. The product was obtained as 6 g (46%) of a white solid. 1H-NMR (300 MHz, CDCl3, ppm): δ 8.01 (m, 1H), 7.89-7.87 (m, 1H), 7.28-7.22 (m, 2H), 3.99 (s, 2H), 2.97-2.72 (m, 8H), 2.28 (s, 3H), 1.13-1.01 (m, 6H). MS (ES, m/z): 265 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09301951B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-caf790e52b57421fbc5fcb5407053606
Quellennotizuspto-grants-2016_04