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Dimethylformamide → 4-(2-Methoxyethenyl) benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 1-Bromo-4-(2-methoxyvinyl)benzene | HCID 53407196 | — |
| 生成物 | 4-(2-Methoxyethenyl) benzaldehyde | HCID 54089612 | — |
反応手順
By the method of example 28, 1-bromo-4-(2-methoxyethenyl)benzene is prepared, lithiated, and reacted with dimethylformamide to provide 4-(2-methoxyethenyl) benzaldehyde as a yellow oil after chromatography. This material is converted to 1-(2-phenylethenyl)-4-(2-methoxyethenyl)benzene by Wittig reaction with benzyl triphenylphosphonium chloride, using the conditions described in example 1 (A). The material is obtained as a mixture of all four possible (E) and (Z) stereoisomers.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464865 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-d13b8a86eb3742028c827cbf275607ac |
| 出典メモ | uspto-grants-1995_11 |