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HRID 433007作成日:2026年10月23日

Allyl bromide → 1,3-Butadienylferrocene

https://huagongshe.com/ja/reaction/433007

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物FerrocenecarboxyaldehydeHCID 15184314—
反応物HCID 178450094HCID 178450094—
反応物HCID 178466060HCID 178466060—
触媒MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物1,3-ButadienylferroceneHCID 129665232—

反応手順

Ferrocenaldehyde or ferrocenyl methyl ketone and allyl bromide are reacted in an ether solvent and in the presence of magnesium metal as a catalyst. The liquid portion of the reaction mixture is introduced into a silica gel column, wherein the weak acidity of the silica gel is able to dehydrate the reaction intermediate 1-ferrocenyl-3-buten-1-ol product. The column is eluted with n-hexane, and after evaporating the solvent from the eluate collected, a purified ferrocenyl-1,3-butadiene product is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664409B1
出典データセットuspto-grants-2003_12
ORD IDord-1873e47b27344b03a5faf5cb04c75af6
出典メモuspto-grants-2003_12