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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 525980생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1-BromooctaneHCID 8140—
반응물Potassium CarbonateHCID 11430—
반응물1,5-DiaminonaphthaleneHCID 16720—
촉매Potassium IodideHCID 4875—
용매1-ButanolHCID 263—
생성물N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamineHCID 6844138238.3%

반응 조건

온도110 °C

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09343198B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e20de384567c4138967ddc336962212b
출처 메모uspto-grants-2016_05