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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 625385생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/625385

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참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1,2-Ethanediamine, N1,N1-diethyl-N2-methyl-HCID 66034—
반응물3-(Bromomethyl)benzoic acidHCID 245650—
용매DimethylformamideHCID 6228—
생성물3-(((2-(Diethylamino)ethyl)(methyl)amino)methyl)benzoic acidHCID 6658683948.8%

반응 조건

온도90 °C

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09301951B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-caf790e52b57421fbc5fcb5407053606
출처 메모uspto-grants-2016_04