<I>tert</I>-Butylation of 1-Naphthol with <I>tert</I>-Butyl Alcohol or <I>tert</I>-Butyl Chloride in the Presence of Sulfuric Acid or Zinc Chloride
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- MIYATA Toshiyuki
- Osaka Municipal Technical Research Institute
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- HAMADA Takahiro
- Tatsumi Chemical Co., Ltd.
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- HIRASHIMA Tsuneaki
- Osaka Municipal Technical Research Institute
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- MANABE Osamu
- Osaka Municipal Technical Research Institute
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- HIYAMA Hachiro
- Osaka Municipal Technical Research Institute
Bibliographic Information
- Other Title
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- 硫酸または塩化亜鉛を触媒とする第3ブチルアルコールあるいは第3塩化ブチルによる1-ナフトールの第3ブチル化
- リュウサン マタハ エンカ アエン オ ショクバイ ト スル ダイ3 ブチルアルコール アルイハ ダイ3 エンカ ブチル ニ ヨル 1-ナフトール ノ ダイ3 ブチルカ
- 1-ナフトールの第3ブチル化反応に関する研究 (第1報)
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Description
tert-Butylation of 1-naphthol with tert-butyl alcohol in acetic acid in the presence of sulfuric acid, and with tert-butyl chloride in tetrachloroethane or chloroform in the presence of anhydrous zinc chloride were studied.<BR>The reaction products were separated and identified.<BR>In the former reaction, the following products were obtained ; 2-tert-butyl-1- naphthol (the main product), 2, 4-di-tert-butyl-1-naphthol, 4-tert-butyl-l-naphthol, 2-tert-butyl-1, 4-naphthoquinone and 3, 3'-di-tert-butyl-4, 4'-dinaphthoquinone.<BR>In the latter, the main product was 3, 6-di-tert-butyl-1-naphthol, and the products described above were also detected.<BR>3, 6-Di-tert-butyl-1-naphthol was obtained in about 40% yield in chloroform, and 4-tert-butyl-l-naphthol was obtained in about 42% yield in tetrachloroethane.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 31 (10), 831-834, 1973
The Society of Synthetic Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282680288886528
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- NII Article ID
- 130000925849
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- NII Book ID
- AN0024521X
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- ISSN
- 18836526
- 00379980
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- NDL BIB ID
- 7651496
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed