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Acetic Acid → 1-(3,5-Dimethoxyphenyl)-2-methyl-4-phenyl-1-butene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Benzyl acetone | HCID 17355 | — |
| 反応物 | (3,5-Dimethoxybenzyl)triphenylphosphonium bromide | HCID 10962038 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(3,5-Dimethoxyphenyl)-2-methyl-4-phenyl-1-butene | HCID 54332096 | — |
反応手順
A solution of n-butyl lithium (29 ml. of 2.2M) is added dropwise to 3,5-dimethoxybenzyl triphenylphosphonium bromide (31.5 g.) in tetrahydrofuran (200 ml.) with stirring and the resulting deep red solution is stirred for one-half hour. Benzyl acetone (9.4 g.) is added dropwise and the reaction mixture stirred for 12 hours. It is then adjusted to pH 7 by addition of acetic acid and concentrated under reduced pressure. The residue is extracted with methylene chloride and the extract evaporated to give crude 1-(3,5-dimethoxyphenyl)-2-methyl-4-phenyl-1-butene as an oil. It is purified by chromatography on silica gel (400 g.) and elution with benzene. Yield: 10 g. as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04143139 |
| 出典データセット | uspto-grants-1979_03 |
| ORD ID | ord-db9ce1adce5c49d292d567985b407e48 |
| 出典メモ | uspto-grants-1979_03 |