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ChemicalBook CAS DataBase List 2-Butyl-4-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-imidazole-5-carboxaldehyde
120568-18-5

2-Butyl-4-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-imidazole-5-carboxaldehyde synthesis

7synthesis methods
-

Yield:120568-18-5 65%

Reaction Conditions:

with potassium phosphate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride in tetrahydrofuran; for 72 h;Product distribution / selectivity;Heating / reflux;

Steps:

9 Example 9

A Schlenk tube was charged with 2-n-butyl-4-chloro-1-[4-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)benzyl)-1H-imidazole-5-carbaldehyde (190 mg), 5-(2-bromophenyl)-1-triphenylmethyl-1H-tetrazole (229 mg), anhydrous K3PO4 (317 mg) and anhydrous tetrahydrofuran (5 mL). The suspension was purged and degassed. Dichloro[1,1-bis(diphenylphosphino)ferrocene]palladium (II) (PdCl2(dppf)) (13 mg) was added, the mixture was purged and degassed. The reaction was refluxed for 72 h. After cooling to room temperature, the reaction mixture was filtered, the cake was washed with dichloromethane. The filtrate and washings were combined and evaporated to dryness. The residue was purified by column chromatography (eluant: cyclohexane/ethyl acetate, 9:1) to yield 212 mg (65%).

References:

EP1833801,2008,B1 Location in patent:Page/Page column 13

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124750-51-2 Synthesis
5-(4'-Bromomethyl-1,1'-biphenyl-2-yl)-1-triphenylmethyl-1H-tetrazole

124750-51-2
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2-Butyl-4-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-imidazole-5-carboxaldehyde

120568-18-5
17 suppliers
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