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HRID 1445559作成日:2026年10月27日

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

https://huagongshe.com/reaction/1445559

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物2-Cyclohexen-1-oneHCID 13594—
反応物2-Chloro-5-ethylpyridine-3-carbaldehydeHCID 24976845—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-oneHCID 5888023895%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666883B2
出典データセットuspto-grants-2010_02
ORD IDord-0a4e91d6deae4e22a91dcc6a58e6c952
出典メモuspto-grants-2010_02