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HRID 68177作成日:2026年10月26日

N,N-bis(3-aminopropyl)methylamine → N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamine

https://huagongshe.com/reaction/68177

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-bis(3-aminopropyl)methylamineHCID 7777—
反応物Sodium CarbonateHCID 10340—
反応物5-Fluoro-2-nitrotolueneHCID 94956—
溶媒TolueneHCID 1140—
生成物N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamineHCID 86731947—

反応条件

温度100 °C

反応手順

To 5-fluoro-2-nitrotoluene (50.0 g, 0.32 mol) was added sodium carbonate (17.1 g, 0.16 mol) at 60° C. 3,3′-Diamino-N-methyldipropylamine (23.7 g, 0.16 mol) was then carefully added dropwise (exothermic reaction). The resulting mixture was heated at 100° C. for 12 hours. 100 ml toluene were added to the cooled reaction mixture causing the inorganic salts to precipitate, which were filtered off. The organic phase was then concentrated down under vacuum in a rotovap to afford the product as a residue in the form of a yellow orange oil. Yield: 52.5 g (78.4%); 1H-NMR (400 MHz, DMSO-d6): δ [ppm]=1.71 (m, 4H); 2.18 (s, 3H); 2.40 (m, 4H); 2.55 (s, 6H); 3.17 (m, 4H); 6.45 (s, 2H); 6.48 (d, 2H); 7.08 (br., 2×NH); 7.92 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08821592B1
出典データセットuspto-grants-2014_09
ORD IDord-727ba28406384fee9d438a866f21cfd8
出典メモuspto-grants-2014_09