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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586652Generated: November 3, 2026

1-Bromooctadecane → 2-Octadecyloxynaphthalene

https://huagongshe.com/reaction/1586652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
Reactant2-NaphtholHCID 8663—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product2-OctadecyloxynaphthaleneHCID 14201680—

Reaction Steps

172.8 g (1.2 mol) 2-naphthol (98%) is added to a solution of 48 g (1.2 mol) sodium hydroxide (99%) in 1 l ethanol in a 4 l three-neck flask with stirrer, cooler and thermometer, after it has dissolved 417 g (1.25 mol) n-octadecylbromide are added and the reaction mixture is heated for 14 hours under reflux. After addition of a further 1 l ethanol the hot solution is aspirated over a Seitz filter to remove inorganic material and the weakly pink coloured filtrate is brought to crystallization by placing it in an ice bath for 30 minutes. After aspiration of the almost colourless crystals, the filter cake is washed in portions with ca. 700 ml ethanol and after drying over diphosphorus pentoxide 371.9 g (93.7% of the theoretical yield) 2-octadecyloxynaphthalene are obtained as colourless crystals, Fp 64°-68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215924
Source datasetuspto-grants-1993_06
ORD IDord-c62ed4fa96f84925b81a9b9880f1d557
Source noteuspto-grants-1993_06