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HRID 1657543作成日:2026年10月27日

p-Menthan-3-one → Piperitenone

https://huagongshe.com/reaction/1657543

反応式

関与物質

役割名称HCID仕込み量
反応物p-Menthan-3-oneHCID 6986—
反応物MenthoneHCID 26447—
生成物PiperitenoneHCID 38115264.6%

反応手順

A similar process is described by S. Ohshiro et al (Yakugaku Zasshi, 88, 417 (1968)). Here again the reaction of methyl vinyl ketone with excess mesityl oxide takes place in the presence of potassium hydroxide powder but without addition of tetrahydrofuran as the solvent. The piperitenone obtained is converted into a mixture of menthone and isomenthone by catalytic hydrogenation. However, in this process of yields of piperitenone are again only about 53%; furthermore, using this process the menthone/isomenthone mixture is obtained in only 64.6% yield and in a purity of only 89.8%. For this reason, the further reaction to give pure methol has to be carried out in an involved manner via menthone-oxime (Jap. Pat. No. 7,009,375) and menthylamine, which makes it doubtful whether the process is suitable for commercial operation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03960970
出典データセットuspto-grants-1976_06
ORD IDord-5299a2cba2b041ffb03ebb7219d2590a
出典メモuspto-grants-1976_06