돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237810생성일: 2026년 10월 27일

4-Cyclohexylphenol → (2S,6R)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one

https://huagongshe.com/reaction/237810

반응식

참여 물질

역할이름HCID투입량
반응물4-CyclohexylphenolHCID 14327—
반응물Ethyl 2-methylidenebutanoateHCID 291416—
반응물(-)-EpichlorohydrinHCID 2734062—
반응물(S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamineHCID 66875140—
용매1-ButanolHCID 263—
생성물(2S,6R)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-oneHCID 25074227—
생성물(2S,6S)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-oneHCID 25074228—

반응 조건

온도90 °C

반응 단계

A solution of (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine (0.85 g, 3.09 mmol), prepared in accordance with the procedures in Steps 1 and 2 of Example 1 and starting from R-epichlorohydrin and 4-cyclohexylphenol, and ethyl ethylacrylate (1.0 g, 7.57 mmol) in n-butanol (2 ml) was heated at 90° C. for 18 hrs. The reaction mixture was concentrated and loaded onto a silica gel column, and eluted with 2-6% isopropanol/methylene chloride to afford (2S,6R)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one (0.24 g) and (2S,6S)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one (0.34 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642603B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7a3f0f1716684aa09e223acbd5c2a242
출처 메모uspto-grants-2014_02