돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1445559생성일: 2026년 10월 27일

Imidazole → 2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-one

https://huagongshe.com/reaction/1445559

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물2-Cyclohexen-1-oneHCID 13594—
반응물2-Chloro-5-ethylpyridine-3-carbaldehydeHCID 24976845—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-oneHCID 5888023895%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666883B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-0a4e91d6deae4e22a91dcc6a58e6c952
출처 메모uspto-grants-2010_02