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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Cyclohexylphenol | HCID 14327 | — |
| 반응물 | Ethyl 2-methylidenebutanoate | HCID 291416 | — |
| 반응물 | (-)-Epichlorohydrin | HCID 2734062 | — |
| 반응물 | (S)-5-(4-cyclohexyl-phenoxymethyl)-4,5-dihydro-oxazol-2-ylamine | HCID 66875140 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | (2S,6R)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one | HCID 25074227 | — |
| 생성물 | (2S,6S)-2-(4-cyclohexyl-phenoxymethyl)-6-ethyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one | HCID 25074228 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08642603B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_02 |
|---|
| ORD ID | ord-7a3f0f1716684aa09e223acbd5c2a242 |
|---|
| 출처 메모 | uspto-grants-2014_02 |
|---|