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1-(4-Chlorophenyl)-2-butyn-1-ol → (Z)-1-(4-chlorophenyl)-2-buten-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(4-Chlorophenyl)-2-butyn-1-ol | HCID 20188339 | — |
| 触媒 | Lindlars catalyst | HCID 131709914 | — |
| 生成物 | (Z)-1-(4-chlorophenyl)-2-buten-1-ol | HCID 67901371 | — |
反応手順
Under nitrogen, hydrogenate a mixture of 10 g (0.055 mole) of 1-(4-chlorophenyl)-2-butyn-1-ol and 0.6 g Lindlar catalyst. Following the reaction vic NMR the reaction is complete in about two days. The hydrogenation is stopped and the reaction stirred under N2 at room temperature overnight. Filter off the catalysts, wash with methylene chloride combine the filtrate and evaporate to yield the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04613609 |
| 出典データセット | uspto-grants-1986_09 |
| ORD ID | ord-1ba35f007e7240af90d3407e16dabfe8 |
| 出典メモ | uspto-grants-1986_09 |