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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DihydroxynaphthaleneHCID 6749—
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product1,5-Bis(octyloxy)naphthaleneHCID 50901175140.2%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09343198B2
Source datasetuspto-grants-2016_05
ORD IDord-9909275f86894bd9a2aaf61545134d1e
Source noteuspto-grants-2016_05