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HRID 1604757作成日:2026年10月26日

2,10-Epoxypinane → Perillyl acetate

https://huagongshe.com/reaction/1604757

反応式

関与物質

役割名称HCID仕込み量
反応物2,10-EpoxypinaneHCID 93046—
反応物Perilla alcoholHCID 369312—
生成物Perillyl acetateHCID 61780—
生成物2,10-EpoxypinaneHCID 93046—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05994598
出典データセットuspto-grants-1999_11
ORD IDord-141cab9e1a1241929399086c3586df2b
出典メモuspto-grants-1999_11