참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4'-Hydroxyacetophenone | HCID 7469 | — |
| 반응물 | Phenyl acetate | HCID 31229 | — |
| 반응물 | alpha-Hydroxyacetophenone | HCID 68490 | — |
| 용매 | Hydrofluoric Acid | HCID 14917 | — |
| 생성물 | 4-Methylphenyl acetate | HCID 8797 | — |
| 생성물 | Guaiacyl acetate | HCID 61155 | — |
| 생성물 | Cresatin | HCID 67406 | — |
반응 단계
Dann and Mylius in a dissertation included as part of a series of Reports from the Institute for Applied Chemistry of the University of Erlangen, received for publication on January 7, 1954 and published in Annalen der Chemie, 587, 1 to 15, show the rearrangement of phenyl acetate in hydrogen fluoride to 4-hydroxyacetophenone, with a maximum yield of 81% after 24 hours of reaction time, and report a yield of 92% stated to be obtained by K. Weichert as reported in Angewandte Chemie, 56, 338 (1943). However, Dann and Mylius suggest that the difference in yields may be at least partly due to the previous ignoring by Weichert of the accompanying 2-hydroxyacetophenone. Dann and Mylius also report somewhat lower yields of hydroxy aromatic ketones from rearrangements in hydrogen fluoride of m-cresyl acetate, p-cresyl acetate, and guaiacol acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04665215 |
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| 출처 데이터셋 | uspto-grants-1987_05 |
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| ORD ID | ord-0fdbe6abf04e4b51be4001a91b7b9f71 |
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| 출처 메모 | uspto-grants-1987_05 |
|---|