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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353391생성일: 2026년 10월 24일

(E)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexyl-2-pentenoic acid → (2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acid

https://huagongshe.com/ko/reaction/353391

반응식

참여 물질

역할이름HCID투입량
반응물(E)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexyl-2-pentenoic acidHCID 22708850—
용매MethanolHCID 887—
생성물(2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acidHCID 983590699.2%

반응 단계

A solution of (E)-2-[2-(teri-butoxy)-2-oxoethyl]-5-cyclohexyl-2-pentenoic acid (0.74 g, 2.5 mmol) and 1,1′-bis[(2S,4S)-2,4-diethylphosphetano]ferrocene-(1,5-cyclooctadiene)-rhodium (I) tetrafluoroborate (18 mg, 25 μmol) in methanol (2.5 ml) was stirred at 20-25° C. for 24 hours, under hydrogen (4 atmospheres, 60 p.s.i.). The mixture was then concentrated in vacuo to leave the title compound as a yellow oil (0.74 g, 98% conversion, enantiomeric excess=95%, 95% pure by NMR).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750363B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-c13e9c1eb2fb41749aada6988c513f03
출처 메모uspto-grants-2004_06