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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 991268생성일: 2026년 10월 27일

Cyclohexene → Oseltamivir

https://huagongshe.com/reaction/991268

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexeneHCID 8079—
반응물Ethyl (3R,4R,5S)-4-acetamido-5-azido-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylateHCID 9967681—
촉매NickelHCID 935—
용매EthanolHCID 702—
생성물OseltamivirHCID 65028—

반응 단계

100 g (0.295 mol) ethyl (3R, 4R, 5S)-4-acetamido-5-azido-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate were dissolved in 800 ml ethanol and placed in a 21 steel autoclave together with 34 g Raney Nickel (Degussa) in 200 ml ethanol. The autoclave was closed rinsed twice with nitrogen and then set under 2 bar hydrogen pressure. Hydrogenation took place at a temperature of 20-25° C. under mechanical stirring a 1000 rpm until, after all the starting material had reacted, also the content of the “2-azido-5-amino intermediate” was ≦0.01% area (GC measurement) which was about 5-8 h. However, it was found that due to this “overhydrogenation” the “cyclohexene double bond” became hydrogenated, too.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06462226B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-a52e8e15df294d5089e7e3f7528627d8
출처 메모uspto-grants-2002_10