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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1604758Erstellt: 25. Oktober 2026

Acetic Anhydride → Perilla alcohol

https://huagongshe.com/reaction/1604758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt2,10-EpoxypinaneHCID 93046—
LösungsmittelAcetic AcidHCID 176—
ProduktPerilla alcoholHCID 369312—

Reaktionsschritte

Among other routes that have been developed to prepare perillyl alcohol from beta pinene oxide is that reported by T. K. Keenan in 1966 who produced perillyl acetate from beta-pinene oxide by refluxing beta-pinene oxide with acetic anhydride and acetic acid for seven hours followed by removal of the acetate to afford a nine percent (9%) yield of perillyl alcohol based on the starting beta-pinene oxide (B.S. Thesis Mass. Institute of Tech.). The applicants found the process to be reproducible albeit in low yield. F. C. Delay in Swiss Patent 5671/84 reported the production of perillyl alcohol in which he treated beta-pinene oxide with nitromethane and ammonium nitrite at a temperature between 20° C. and 90° C. in an overall yield of thirty percent (30%). Two years later Wang and co-workers published in Tetrahedron 1986, 620-638 complete details of this procedure and reported an overall yield of sixty-eight percent (68%) perillyl alcohol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05994598
Quelldatensatzuspto-grants-1999_11
ORD IDord-bfd85e66572b4d889adea2b672358d80
Quellennotizuspto-grants-1999_11