HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463771Generated: October 30, 2026
1-Bromooctadecane → 2-Octadecyloxynaphthalene
https://huagongshe.com/reaction/1463771
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromooctadecane | HCID 8218 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Octadecyloxynaphthalene | HCID 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-naphthyl-octadecyl-ether are obtained as colourless crystals, Fp 64°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302346 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-67a0762bdfc54bb884f9ddd3203723a8 |
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| Source note | uspto-grants-1994_04 |
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