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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358284생성일: 2026년 10월 25일

2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acid → Fenoprofen

https://huagongshe.com/reaction/358284

반응식

참여 물질

역할이름HCID투입량
반응물2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acidHCID 20449833—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
생성물FenoprofenHCID 334289%

반응 단계

To a solution of 4.1 g. of 2-toluene-sulphonyloxy-3-phenoxy-hydratropic acid in 150 ml. of alcohol 24 g. of a W-6 nickel catalyst are added, and the mixture is hydrogenated at 25° C., under atmospheric pressure until a calculated amount of hydrogen is used up. The catalyst is filtered off, the filtrate is evaporated and the residue is taken up in water and acidified with a 10% aqueous hydrochloric acid solution. The separated oil is extracted with chloroform, the chloroform solution is dried over sodium sulphate and evaporated. 2.1 g. (89%) of 3-phenoxy-hydratropic acid are obtained. Melting point of the corresponding cyclohexylamine salt amounts to 151° C. to 153° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04465855
출처 데이터셋uspto-grants-1984_08
ORD IDord-f3f0daef5bb3420fb5df1f9d4d60a4da
출처 메모uspto-grants-1984_08