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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525980Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromooctaneHCID 8140—
EduktPotassium CarbonateHCID 11430—
Edukt1,5-DiaminonaphthaleneHCID 16720—
KatalysatorPotassium IodideHCID 4875—
Lösungsmittel1-ButanolHCID 263—
ProduktN1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamineHCID 6844138238,3%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09343198B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-e20de384567c4138967ddc336962212b
Quellennotizuspto-grants-2016_05