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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49393생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/49393

반응식

참여 물질

역할이름HCID투입량
반응물1,4-CyclohexadieneHCID 12343—
반응물Benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl]-carbamateHCID 20587951—
생성물2-[4-(2-Methyl-oxazol-4-yl)-phenoxy]-ethylamineHCID 9813220100.9%

반응 단계

A round-bottomed flask containing benzyl-{2-[4-(2-methyl-oxazol-4-yl)-phenoxy]-ethyl}-carbamate (788 mg, 2.07 mmol) was purged with nitrogen, and 10% Pd/C (200 mg, 20 wt %), ethyl acetate (15 ml), and methanol (5 ml) were added. 1,4-cyclohexadiene (0.90 ml, 9.60 mmol) was then added to the mixture, and the solution was allowed to stir at room temperature for about one hour. The reaction mixture was then filtered through a pad of diatomaceous earth and the filter cake was washed with methanol. The filtrate was concentrated in vacuo and the residue purified by column chromatography (silica gel; methylene chloride to 20% methanol/methylene chloride) to afford 456 mg (89% yield) of the desired product. LRMS ([M+H]+)=247.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706743B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-cab500ab5a86490caef9a39eb4c7cefb
출처 메모uspto-grants-2004_03