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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49373생성일: 2026년 10월 25일

1,4-Cyclohexadiene → 2-[4-(4-Methyl-oxazol-2-yl)-phenoxy]-ethylamine

https://huagongshe.com/reaction/49373

반응식

참여 물질

역할이름HCID투입량
반응물1,4-CyclohexadieneHCID 12343—
반응물{2-[4-(4-Methyl-oxazol-2-yl)-phenoxy]-ethyl}-carbamic acid benzyl esterHCID 12986049—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물2-[4-(4-Methyl-oxazol-2-yl)-phenoxy]-ethylamineHCID 1207199790%

반응 단계

The title compound of Example 1, {2-[4-(4-Methyl-oxazol-2-yl)-phenoxy]-ethyl}-carbamic acid benzyl ester, (166 mg, 0.47 mmol) was dissolved in methanol (5 ml) and 10% Pd/C (50 mg) and 1,4-cyclohexadiene (192 mg, 2.4 mmol) were added to the resulting solution. The mixture was allowed to stir for about sixteen hours, and then it was filtered through diatomaceous earth, and the filter pad was washed with methanol. The filtrate was concentrated in vacuo to dryness, and the resulting material (92 mg, 90% yield), which was determined to be pure by 1H NMR, was used directly without further purification. LRMS ([M+H]+)=219.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706743B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-b8a149b034b44dceb24886fdb7e850f7
출처 메모uspto-grants-2004_03