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HRID 625385作成日:2026年10月26日

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

https://huagongshe.com/reaction/625385

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物1,2-Ethanediamine, N1,N1-diethyl-N2-methyl-HCID 66034—
反応物3-(Bromomethyl)benzoic acidHCID 245650—
溶媒DimethylformamideHCID 6228—
生成物3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acidHCID 6658683948.8%

反応条件

温度90 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09301951B2
出典データセットuspto-grants-2016_04
ORD IDord-caf790e52b57421fbc5fcb5407053606
出典メモuspto-grants-2016_04