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Carboxylation of Active Methylene Compounds with Base-Magnesium Chloride-Carbon Dioxide Mixtures
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- MATSUMURA Noboru
- Department of Applied Chemistry, College of Engineering, University of Osaka Prefecture
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- YAGYU Yoshio
- Department of Applied Chemistry, College of Engineering, University of Osaka Prefecture
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- IMOTO Eiji
- Department of Applied Chemistry, College of Engineering, University of Osaka Prefecture
Bibliographic Information
- Other Title
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- 塩基-塩化マグネシウムー二酸化炭素系による活性メチレン化合物のカルボキシル化
- 塩基‐塩化マグネシウム‐二酸化炭素系による活性メチレン化合物のカルボキシル化
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Description
Various binary mixtures consisting of a base and magnesium chloride promote the carboxylation of various kinds of active methylene compounds with carbon dioxide. Monocarboxylic acid is obtained as a only product in excellent yield. The reactions are promoted by such a strong tertiary amine as triethylamine or triethylenediamine, but not by such a weak tertiary amine as pyridine or N, N-dimethylaniline. Primary or secondary amines are not effective. Among the chlorides of uni-, bi-, and tri-valent metals, magnesium chloride is the most effective substance to promote the carboxylation of indene or acetophenone.
Journal
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- NIPPON KAGAKU KAISHI
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NIPPON KAGAKU KAISHI 1977 (9), 1344-1348, 1977-09-10
The Chemical Society of Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282679395176192
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- NII Article ID
- 130004156014
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- COI
- 1:CAS:528:DyaE1cXmsFyk
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- ISSN
- 21850925
- 03694577
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed