参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 1-溴辛烷 | HCID 8140 | — |
| 反应物 | 碳酸钾 | HCID 11430 | — |
| 反应物 | 1,5-萘二胺 | HCID 16720 | — |
| 催化剂 | 碘化钾 | HCID 4875 | — |
| 溶剂 | 丁醇 | HCID 263 | — |
| 产物 | N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine | HCID 68441382 | 38.3% |
反应步骤
Naphthalene-1,5-diamine (3.14 g, 19.8 mmol), 1-bromooctane (25.25 g, 0.130 mol), potassium carbonate (11.79 g, 85.3 mmol), and potassium iodide (0.05 g, 0.30 mmol) was stirred in dry butanol (150 ml) and heated to 110° C. for 36 h. The reaction was quenched with water and extracted with ether three times. The combined organic phase was washed three times with water and evaporated to give black oil which was distilled under reduced pressure at 90° C. to yield a black tar. This was purified with flash chromatography using hexane as mobile phase to obtain colourless oil which crystallised to yield N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine (2.3 g, 3.79 mmol) as white crystals. 1H-NMR (CDCl3, δ): 0.85 (t, 12H), 1.0-1.4 (m, 40H), 1.4-1.6 (m, 8H), 3.08 (t, 8H), 7.1 (d, 2H), 7.35 (t, 2H), 8.01 (d, 2H) MS MALDI-TOF (m/z): 606.574
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US09343198B2 |
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| 来源数据集 | uspto-grants-2016_05 |
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| ORD ID | ord-e20de384567c4138967ddc336962212b |
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| 来源说明 | uspto-grants-2016_05 |
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