化工社化工社 化学情報印刷レポート · 研究参考用
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5-Fluoro-2-nitrotoluene | HCID 94956 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamine | HCID 86731947 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08821592B1 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-727ba28406384fee9d438a866f21cfd8 |
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| 出典メモ | uspto-grants-2014_09 |
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