Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525981Erstellt: 26. Oktober 2026

1,5-Dihydroxynaphthalene → 1,5-Bis(octyloxy)naphthalene

https://huagongshe.com/reaction/525981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,5-DihydroxynaphthaleneHCID 6749—
Edukt1-BromooctaneHCID 8140—
EduktPotassium CarbonateHCID 11430—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,5-Bis(octyloxy)naphthaleneHCID 50901175140,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09343198B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-9909275f86894bd9a2aaf61545134d1e
Quellennotizuspto-grants-2016_05