戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1370775作成日:2026年10月27日

Acetone → 6-Methyl-2-heptanone

https://huagongshe.com/reaction/1370775

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物3-MethylbutanalHCID 11552—
生成物6-Methyl-2-heptanoneHCID 13572—

反応手順

To aid comprehension, the reaction will be explained here by the example of the reaction of acetone with isovaleraldehyde to produce 6-methylheptan-2-one. The reaction takes place “in situ” via the stage of aldol condensation with the formation of the corresponding β-hydroxyketone, which is not isolated. Dehydration to 6-methylhept-3-en-2-one takes place under the reaction conditions, and this is hydrogenated selectively to the corresponding methylketone with the hydrogenation catalyst distributed homogeneously in the aqueous catalyst phase.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06583323B2
出典データセットuspto-grants-2003_06
ORD IDord-f282adfabe8d45cda6642831763bf31f
出典メモuspto-grants-2003_06