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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1657543Erstellt: 26. Oktober 2026

p-Menthan-3-one → Piperitenone

https://huagongshe.com/reaction/1657543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Menthan-3-oneHCID 6986—
EduktMenthoneHCID 26447—
ProduktPiperitenoneHCID 38115264,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03960970
Quelldatensatzuspto-grants-1976_06
ORD IDord-5299a2cba2b041ffb03ebb7219d2590a
Quellennotizuspto-grants-1976_06