HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612800Generated: November 1, 2026
Hydrochloric Acid → 2-Butyl-1-(4-iodobenzyl)imidazol-4,5-dicarboxylic acid
https://huagongshe.com/reaction/612800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Iodobenzyl bromide | HCID 954258 | — |
| Reactant | Dimethyl 2-butyl-1H-imidazole-4,5-dicarboxylate | HCID 14955796 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Butyl-1-(4-iodobenzyl)imidazol-4,5-dicarboxylic acid | HCID 19596418 | 87.6% |
Reaction Steps
Dimethyl 2-butylimidazol-4,5-dicarboxylic acid (7.12 g, 29.6 mmol) and 4-iodobenzyl bromide (10.56 g, 35.5 mmol) were dissolved in DMF (50 ml), and 60% oily sodium hydride (1.3 g, 32.5 mmol) was added in small portions while stirring at room temperature. The reaction solution was stirred at room temperature for 2 hours and methanol was added to treat excess sodium hydride. Then the reaction solution was neutralized with 2N HCl and the product was extracted with dichloromethane. The extracted solution was dried over sodium sulfate and concentrated in reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to give the titled compound (11.1 g, 82%) as a tan solid (mp:98-99° C., Rf:0.60 silica gel-ethyl acetate/hexane/=1/1). This has the following NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005105 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-cdf31f20f8224348856ae100cc0069cf |
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| Source note | uspto-grants-1999_12 |
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