関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Pyridinylacetone | HCID 80552 | — |
| 反応物 | Cinnamaldehyde | HCID 637511 | — |
| 触媒 | Acetic Acid | HCID 176 | — |
| 触媒 | Piperidine | HCID 8082 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-Phenyl-3-(4-pyridinyl)hexa-3,5-dien-2-one | HCID 53898926 | 17% |
反応手順
Trans-cinnamaldehyde (1.84 ml, 14.8 mmol), five drops of piperidine and five drops of acetic acid were added to a solution of 4-pyridyl acetone (2.0 g, 14.8 mmol) in toluene (25 ml). The mixture was heated to reflux for 48 hours with a Dean-Stark trap to remove water. The mixture was concentrated to give a black oil. The oil was purified by silica gel chromatography (eluted with 1:1 hexane/ethyl acetate). The desired fractions were collected, combined and concentrated to give 6-phenyl-3-(4-pyridinyl)hexa-3,5-dien-2-one (628 mg). The ketone was further purified by an additional column chromatography on silica gel (eluting with hexane-ethyl acetate-methylene chloride-methanol (1:1:2:0.12)) (380 mg, 27.3%): Anal. Calc'd for C17H15NO 0.4 H2O: C, 79.91; H, 5.84; N, 5.48. Found: C, 79.72; H, 5.91; N, 5.25. MS (M+H+): 250.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852740B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-76f21bb7c71f40d295b3b5201fb179c3 |
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| 出典メモ | uspto-grants-2005_02 |
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