HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525981Generated: October 26, 2026
1,5-Dihydroxynaphthalene → 1,5-Bis(octyloxy)naphthalene
https://huagongshe.com/reaction/525981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dihydroxynaphthalene | HCID 6749 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,5-Bis(octyloxy)naphthalene | HCID 50901175 | 140.2% |
Reaction Steps
1,5-dihydroxynaphthalene (2.95 g, 18.4 mmol), 1-bromooctane (8.2 g, 42.5 mmol), and potassium carbonate (50 g, 0.36 mol) was mixed in N,N-dimethylformamide and heated at 90° C. for 5 h. The potassium carbonate was filtered off and the reaction mixture was quenched with water and extracted two times with ether. The combined organic phase was then washed once with 1M HCl, two times with water, and evaporated. The residual brown solid was recrystallised in ethanol to form 1,5-bis(octyloxy)naphthalene (4.96 g, 12.9 mmol) as brown crystals. 1H-NMR (CDCl3, δ): 0.89 (t, 6H), 1.2-1.4 (m, 16H), 1.4-1.6 (m, 4H), 1.91 (m, 4H), 4.12 (t, 4H), 6.81 (d, 2H), 7.34 (t, 2H), 7.83 (d, 2H) MS MALDI-TOF (m/z): 384.266
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-9909275f86894bd9a2aaf61545134d1e |
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| Source note | uspto-grants-2016_05 |
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