@article{oai:kanazawa-u.repo.nii.ac.jp:00011829,
 author = {Suda, Hiroshi and Higashi, Hirofumi and 隅田, 弘 and 東, 宏文},
 issue = {4},
 journal = {金沢大学工学部紀要 = Memoirs of the Faculty of Technology Kanazawa University},
 month = {Nov},
 note = {In order to synthesize 6-alkyl-2-naphthols which should be expected to be intermediates of azo dyestuff for synthetic fibre as polypropylene, β-naphthyl ethylether were acylated by the reaction of Friedel Crafts using aluminium chloride and five acyl chlorides, that is, acetyl, propionyl, n-butyryl, n-valeryl and n-caproyl in nitrobenzene.
Then, their carbonyl groups were reduced by the Huang-Minlon method.
The final objects were obtained by boiling them with hydroiodic acid to break the ether bond. 
Each process resulted in good yield.},
 pages = {119--125},
 title = {アルキル-β-ナフトールの合成},
 volume = {3},
 year = {1964}
}