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ChemicalBook CAS DataBase List 5-IODO-1H-BENZIMIDAZOLE
78597-27-0

5-IODO-1H-BENZIMIDAZOLE synthesis

1synthesis methods
Formic acid

64-18-6

4-Iodo-2-nitroaniline

20691-72-9

5-IODO-1H-BENZIMIDAZOLE

78597-27-0

The general procedure for the synthesis of 5-iodobenzimidazole from formic acid and 4-iodo-2-nitroaniline is as follows: intermediate Example 12.Synthesis of 5-iodo-1H-benzo[d]imidazole from 5-((trimethylsilyl)ethynyl)-1H-benzo[d]imidazole). 4-Methyl-2-nitroaniline (1 g, 3.7 mmol) was dissolved in formic acid (10 ml), iron powder (2.1 g, 37 mmol) was added, and the reaction mixture was heated and refluxed for 12 h at 90 °C. After completion of the reaction, formic acid was removed by distillation. The crude product was dissolved in ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, and then dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to afford the target product 5-iodo-1H-benzo[d]imidazole in 68% yield (0.85 g). Product characterization by LC-MS (ES): calculated mass: 243.95; observed mass: 244.8 [M + H]+ (retention time: 0.173 min).

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Yield:78597-27-0 68%

Reaction Conditions:

with iron at 90; for 12 h;

Steps:

12.a a) 5-lodo- 1H-benzo[djimidazole
Intermediate Example 12.5-((Trimethylsilyl)ethynyl)- 1H-benzo[d]imidazolea) 5-lodo- 1H-benzo[djimidazoleTo a solution 4-ioclo-2-nitroaniline (1 g, 3.7mmol) in formic acid (10 ml), iron(2.1 g, 37 mmol) was added and heated at 90°C for 12 h. The formic acid was distilledoff and the crude was dissolved in ethyl acetate. The ethyl acetate layer was washed with water, brine and dried over sQdiurn sulphate. The solvent was distilled off to afford the title product in 68 %. yield (0.85 g)..LC-MS (ES]): Calculated mass: 243.95; Observed mass: 244.8 [M+H} + (rt: 0.173 mm).

References:

ORION CORPORATION;RAJAGOPALAN, Srinivasan;APPUKUTTAN, Prasad;NARASINGAPURAM ARUMUGAM, Karthikeyan;UJJINAMATADA, Ravi Kotrabasaiah;GEORGE, Shyla;LINNANEN, Tero WO2014/162039, 2014, A1 Location in patent:Page/Page column 39

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