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HRID 978794생성일: 2026년 10월 24일

4'-Hydroxyacetophenone → 4-Methylphenyl acetate

https://huagongshe.com/ko/reaction/978794

반응식

참여 물질

역할이름HCID투입량
반응물4'-HydroxyacetophenoneHCID 7469—
반응물Phenyl acetateHCID 31229—
반응물alpha-HydroxyacetophenoneHCID 68490—
용매Hydrofluoric AcidHCID 14917—
생성물4-Methylphenyl acetateHCID 8797—
생성물Guaiacyl acetateHCID 61155—
생성물CresatinHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04665215
출처 데이터셋uspto-grants-1987_05
ORD IDord-0fdbe6abf04e4b51be4001a91b7b9f71
출처 메모uspto-grants-1987_05