A Preparative Method of Allylketones from Esters of Carboxylic Acids
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- SUGA Kyoichi
- Department of Applied Chemistry, Faculty of Engineering, Chiba University
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- WATANABE Shoji
- Department of Applied Chemistry, Faculty of Engineering, Chiba University
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- FUJITA Tsutomu
- Department of Applied Chemistry, Faculty of Engineering, Chiba University
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- KURAMOCHI Tadao
- Department of Applied Chemistry, Faculty of Engineering, Chiba University
Bibliographic Information
- Other Title
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- カルボン酸からアリルケトンの合成
- カルボンサン カラ アリルケトン ノ ゴウセイ
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Description
Various allyl ketones were prepared from esters via two steps : Grignard reaction of allylmagnesium chloride with esters and thermolysis of the resulted diallyl alcohol. For example, 4-allyl-1-decen-4-ol (2) was prepared from methylheptanate (1) and allylmagnesium chloride. At 440°C and atmospheric pressure, compound (2) thermally decomposes to 1-decen-4-one (3).
Journal
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- Journal of Japan Oil Chemists' Society
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Journal of Japan Oil Chemists' Society 26 (12), 792-793, 1977
Japan Oil Chemists' Society
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Details 詳細情報について
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- CRID
- 1390282680308174720
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- NII Article ID
- 130001014602
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- NII Book ID
- AN00245435
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- ISSN
- 0513398X
- 18842003
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- NDL BIB ID
- 1855781
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed