Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604757Generated: October 25, 2026

2,10-Epoxypinane → Perillyl acetate

https://huagongshe.com/reaction/1604757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,10-EpoxypinaneHCID 93046—
ReactantPerilla alcoholHCID 369312—
ProductPerillyl acetateHCID 61780—
Product2,10-EpoxypinaneHCID 93046—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994598
Source datasetuspto-grants-1999_11
ORD IDord-141cab9e1a1241929399086c3586df2b
Source noteuspto-grants-1999_11