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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,5-Diaminonaphthalene | HCID 16720 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine | HCID 68441382 | 38.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09343198B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e20de384567c4138967ddc336962212b |
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| Source note | uspto-grants-2016_05 |
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