참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,10-Epoxypinane | HCID 93046 | — |
| 반응물 | Perilla alcohol | HCID 369312 | — |
| 생성물 | Perillyl acetate | HCID 61780 | — |
| 생성물 | 2,10-Epoxypinane | HCID 93046 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05994598 |
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| 출처 데이터셋 | uspto-grants-1999_11 |
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| ORD ID | ord-141cab9e1a1241929399086c3586df2b |
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| 출처 메모 | uspto-grants-1999_11 |
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