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Imidazole → 2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | 2-Cyclohexen-1-one | HCID 13594 | — |
| 反応物 | 2-Chloro-5-ethylpyridine-3-carbaldehyde | HCID 24976845 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-[(2-Chloro-5-ethylpyridine-3-yl)(hydroxy)methyl]cyclohex-2-ene-1-one | HCID 58880238 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07666883B2 |
| 出典データセット | uspto-grants-2010_02 |
| ORD ID | ord-0a4e91d6deae4e22a91dcc6a58e6c952 |
| 出典メモ | uspto-grants-2010_02 |