Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → 2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | 2-Cyclohexen-1-one | HCID 13594 | — |
| 반응물 | 2-Chloro-5-ethylpyridine-3-carbaldehyde | HCID 24976845 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-one | HCID 58880238 | 95% |
반응 단계
The clear solution of 2-Chloro-5-ethylnicotinaldehyde (10 mmol, 1.69 g) and imidazole (10 mmol) in 50 ml. of MeOH was slowly charged with 50 ml. of deionized water. To a stirred homogeneous reaction mixture was added 2-cyclohexen-1-one (10.2 mmol., 1.0 g) at room temperature and reaction progress was monitored by TLC. Upon completion of the reaction, excess MeOH was removed under reduced pressure, washed with water and extracted with CHCl3 thrice. Combined organic layers were washed with brine solution twice. The organic layer was concentrated and column chromatography of the crude product on silica gel, using 30% EtOAC in hexane as eluent, gave pure Baylis-Hillman adduct in 95% yield (2.43 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07666883B2 |
| 출처 데이터셋 | uspto-grants-2010_02 |
| ORD ID | ord-0a4e91d6deae4e22a91dcc6a58e6c952 |
| 출처 메모 | uspto-grants-2010_02 |