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Piperidine → (E)-1-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(indol-3-yl)-2-propen-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | Indole-3-Carboxaldehyde | HCID 10256 | — |
| 反応物 | Acetosyringone | HCID 17198 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (E)-1-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(indol-3-yl)-2-propen-1-one | HCID 21850208 | 19.2% |
反応手順
4'-Hydroxy-3',5'-dimethoxyacetophenone (1.96 g) and indole-3-carboxaldehyde (1.45 g) were dissolved in ethanol (20 ml), and piperidine (0.85 g) was added thereto, followed by heating under reflux for 32 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography. The obtained crude crystals were recrystallized from ethyl acetate to give Compound 70 (0.62 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05952355 |
| 出典データセット | uspto-grants-1999_09 |
| ORD ID | ord-74a841b976bc4f10a9a9ce9d1f52035d |
| 出典メモ | uspto-grants-1999_09 |