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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237753생성일: 2026년 10월 24일

4-Cyclohexylphenol → (S)-2-(4-cyclohexyl-phenoxymethyl)-5-ethyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one

https://huagongshe.com/ko/reaction/237753

반응식

참여 물질

역할이름HCID투입량
반응물4-CyclohexylphenolHCID 14327—
반응물Ethyl pent-2-yn-1-oateHCID 99169—
반응물(-)-EpichlorohydrinHCID 2734062—
반응물(S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamineHCID 66875140—
용매EthanolHCID 702—
생성물(S)-2-(4-cyclohexyl-phenoxymethyl)-5-ethyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-oneHCID 25074223—

반응 단계

To a solution of (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine (1.0 g, 3.64 mmol), prepared in accordance with the procedures as set forth in Steps 1 and 2 of Example 1 and starting from R-epichlorohydrin and 4-cyclohexylphenol, in ethanol (18.2 mL) was added ethyl 2-pentynoate (0.92 g, 7.28 mmol). The reaction mixture was heated at reflux for 14 hrs and then gradually cooled to room temperature. The resulting crystalline solid was isolated by filtration, washed with heptane 3 times, and dried under vacuum to afford 560 mg of (S)-2-(4-cyclohexyl-phenoxymethyl)-5-ethyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one as a white solid. [α]D25 −27.96 (c 0.526, CHCl3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642603B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-1892876516164c2fa586556fdba07101
출처 메모uspto-grants-2014_02