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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525980Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
Reactant1,5-DiaminonaphthaleneHCID 16720—
CatalystPotassium IodideHCID 4875—
Solvent1-ButanolHCID 263—
ProductN1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamineHCID 6844138238.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09343198B2
Source datasetuspto-grants-2016_05
ORD IDord-e20de384567c4138967ddc336962212b
Source noteuspto-grants-2016_05