6-シアノヘキサン酸の接触遷元
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概要
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Reduction of 6-cyanohexanoic acid, obtained by the reaction of ε-caprolactone with alkali metal cyanide, was studied with cobalt or nickel catalysts. Cobalt catalysts such as Raney Co and Urushibara Co gave 7- aminoheptanoic acid in high yields in dilute ammonia solutions. On the other hand nickel catalysts gave much more iminodiheptanoic acid and much less ω-amino acid. In addition, separation of nickel ion generated in the reaction was more difficult than that of cobalt ion. Some other ω-amino acids were obtained by the above-mentioned operation.
- 社団法人 有機合成化学協会の論文
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関連論文
- ε-カプロラクトンとアンモニア水の反応 γ-およびδ-カプロラクタムの生成(ノート)
- ε-カプロラクトンとシアン化アルカリの反応
- 2-(β-Cyanoethyl)cyclohexanone (有機化合物合成法)
- 高分子工業における原料問題
- 6-シアノヘキサン酸の接触遷元