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HRID 525980作成日:2026年10月23日

1-Bromooctane → N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine

https://huagongshe.com/ja/reaction/525980

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromooctaneHCID 8140—
反応物Potassium CarbonateHCID 11430—
反応物1,5-DiaminonaphthaleneHCID 16720—
触媒Potassium IodideHCID 4875—
溶媒1-ButanolHCID 263—
生成物N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamineHCID 6844138238.3%

反応条件

温度110 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09343198B2
出典データセットuspto-grants-2016_05
ORD IDord-e20de384567c4138967ddc336962212b
出典メモuspto-grants-2016_05