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HRID 363386作成日:2026年10月25日
Bis(3-aminopropyl)amine → Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine
https://huagongshe.com/reaction/363386
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Bis(3-aminopropyl)amine | HCID 5942 | — |
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine | HCID 373797 | 59% |
反応手順
To a stirred solution of p-toluenesulfonyl chloride (240 g, 1.26 mole) in pyridine (600 ml) at 0° C. was added a solution of 1,5,9-triazanonane (50.0 g, 0.381 mole) in pyridine (100 ml) under a dry nitrogen atmosphere, maintaining the temperature ≤60° C. The addition required 15 minutes. The solvent was removed in vacuo and the resulting yellow oil was dissolved in ethyl acetate (1 l) and H2O (500 ml). The ethyl acetate layer was separated, washed with 0.1N HCl, H2O and saturated NaCl solution and dried (MgSO4). The solution was decolorized with silica gel and the solvent was removed in vacuo to give 133 g (59% yield) of the crude product as a glassy solid: 1H NMR (CDCl3) δ 1.71 (quint, J=6.6 Hz, 4 H), 2.42 (s, 6 H), 2.43 (s, 3 H), 2.96 (quart, J=6.4 Hz, 4 H), 3.11 (t, J=6.8 Hz, 4 H), 5.12 (t, J=6.6 Hz, 2 H), 7.30 (m, 6 H), 7.63 (m, 2 H), 7.73 (m, 4 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05874421 |
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| 出典データセット | uspto-grants-1999_02 |
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| ORD ID | ord-74d5eaa312b44262b58faba2559a5680 |
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| 出典メモ | uspto-grants-1999_02 |
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