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The Synthesis of alky1-β-naphthols
Bibliographic Information
- Other Title
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- アルキル-β-ナフトールの合成
- アルキル-ベータ-ナフトール ノ ゴウセイ
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Description
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.
Journal
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- 金沢大学工学部紀要 = Memoirs of the Faculty of Technology Kanazawa University
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金沢大学工学部紀要 = Memoirs of the Faculty of Technology Kanazawa University 3 (4), 119-125, 1964-11-01
1964-11-01
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Details 詳細情報について
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- CRID
- 1390578061483069952
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- NII Article ID
- 120002661923
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- NII Book ID
- AN00044309
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- ISSN
- 0022832X
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- HANDLE
- 2297/25812
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- NDL BIB ID
- 8146138
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- Text Lang
- ja
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- Article Type
- departmental bulletin paper
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- Data Source
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- JaLC
- IRDB
- NDL Search
- CiNii Articles
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- Abstract License Flag
- Allowed