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HRID 354227作成日:2026年10月27日

1-Ethyl-3-methylimidazolium chloride → n-Carboxymethyl-3,4,5,6-tetrahydroaniline

https://huagongshe.com/reaction/354227

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-methylimidazolium chlorideHCID 2734160—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物n-Carboxymethyl-3-amino-1,7-octadieneHCID 23513356—
触媒RutheniumHCID 23950—
触媒HCID 178420536HCID 178420536—
溶媒HexaneHCID 8058—
生成物n-Carboxymethyl-3,4,5,6-tetrahydroanilineHCID 21559099—

反応手順

92 mg (0.5 mmol) of N-carboxymethyl-3-amino-1,7-octadiene and 10 mg of the ruthenium catalyst shown in the reaction scheme above, namely (tricyclohexylphosphine)-benzylidene-chloro-ruthenium-(IV) 2-[(2,6-diisopropylphenyl)imino]methyl-4-nitro-phenoxide, were dissolved in 1 ml of absolute hexane and a mixture of 290 mg (2 mmol) of 1-methyl-3-ethylimidazolium chloride and 266 mg (2 mmol) of aluminium trichloride under an argon atmosphere in a baked-out Schlenk tube. The mixture was allowed to react for 3 hours at 50° C. For the work-up, the organic phase was pipetted off and the phase comprising the ionic liquid was washed twice with 2 ml each time of hexane. The combined hexane phases were evaporated. Finally, the mixture was filtered through a very short silica gel column (0.2 cm), washed once with 1 ml of acetonitrile and evaporated. The catalyst dissolved in the ionic liquid is available for a further reaction with substrate in hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756500B1
出典データセットuspto-grants-2004_06
ORD IDord-a7eb0473c5b84420a42ca0e8460f7f59
出典メモuspto-grants-2004_06