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HRID 525980生成日期:2026年10月23日

1-溴辛烷 → N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine

https://huagongshe.com/zh-CN/reaction/525980

反应方程式

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-diamineHCID 6844138238.3%

反应条件

温度110 °C

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

DOI10.6084/m9.figshare.5104873.v1
专利号US09343198B2
来源数据集uspto-grants-2016_05
ORD IDord-e20de384567c4138967ddc336962212b
来源说明uspto-grants-2016_05