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3-Phenylprop-2-Enal → 2-(2-Hydroxy-4-phenyl-3-buten-1-yl)-6-methylpyrazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Phenylprop-2-Enal | HCID 307 | — |
| 反応物 | 2,6-Dimethylpyrazine | HCID 7938 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(2-Hydroxy-4-phenyl-3-buten-1-yl)-6-methylpyrazine | HCID 54402095 | — |
反応手順
To a solution of lithium diisopropylamide (1.5 Molar, 73.3 mL, 0.11 mole) in 150 mL of tetrahydrofuran at -78° C. is added slowly a solution of 2,6-dimethylpyrazine (10.8 g, 0.1 mole) in 100 mL of tetrahydrofuran. The mixture is allowed to warm to room temperature and then cooled to -78° C. A solution of cinnamaldehyde (14.5 g, 0.11 mole) in 100 mL of tetrahydrofuran is added dropwise over 15 minutes. The reaction product mixture is then worked up according to the procedures of Example I to provide the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05218118 |
| 出典データセット | uspto-grants-1993_06 |
| ORD ID | ord-2fd2c05a8d0540feb03b78804db9d027 |
| 出典メモ | uspto-grants-1993_06 |