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HRID 249569作成日:2026年10月26日

Bis(eta-cyclopentadienyl) iron → Bis(eta-cyclopentadienyl) iron

https://huagongshe.com/reaction/249569

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(eta-cyclopentadienyl) ironHCID 7611—
反応物Stannous ChlorideHCID 24479—
反応物HCID 178520619HCID 178520619—
反応物HCID 178520620HCID 178520620—
触媒Adams' catalystHCID 345198—
触媒Aluminum(III) ChlorideHCID 6451240—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
生成物Bis(eta-cyclopentadienyl) ironHCID 7611—
生成物4-Chlorobutyryl chlorideHCID 78370—
生成物HCID 178520619HCID 178520619—

反応手順

In an inert atmosphere, 170 mg of PtO2.xH2O (containing 80% of Pt) and 5 mg of anhydrous SnCl2 are introduced into the glass beaker. 120 cm3 of glacial acetic acid and 29.1 g (0.10 mol) of 4-chlorobutyroylferrocene whose main impurities are 1.4% by weight of ferrocene and 0.88% by weight of 1,1'-di(4-chlorobutyroyl)ferrocene are then poured in. This 4-chlorobutyroylferrocene was obtained in the customary manner by a reaction of the Friedel-Crafts type between ferrocene and 4-chlorobutyryl chloride in CH2Cl2 in the presence of AlCl3 as catalyst, followed by recrystallisation of the crude product obtained from hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05214175
出典データセットuspto-grants-1993_05
ORD IDord-7535c6cada5e4d8aa4c298bdb54a4fc2
出典メモuspto-grants-1993_05