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HRID 1789457作成日:2026年10月27日

1-(4-Chlorophenyl)-2-butyn-1-ol → (Z)-1-(4-chlorophenyl)-2-buten-1-ol

https://huagongshe.com/reaction/1789457

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Chlorophenyl)-2-butyn-1-olHCID 20188339—
触媒Lindlars catalystHCID 131709914—
生成物(Z)-1-(4-chlorophenyl)-2-buten-1-olHCID 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 via 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04689341
出典データセットuspto-grants-1987_08
ORD IDord-93abc6b367ac4c85828867dcc8b49366
出典メモuspto-grants-1987_08