HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538841Generated: October 30, 2026
Dimethylformamide → 2-(4-bromobenzyl)-1-propyl-1H-imidazole-4-carboxylic acid ethyl ester
https://huagongshe.com/reaction/538841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | HCID 178469892 | HCID 178469892 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-bromobenzyl)-1-propyl-1H-imidazole-4-carboxylic acid ethyl ester | HCID 58088907 | 33.6% |
| Product | 2-(4-bromobenzyl)-3-propyl-3H-imidazole-4-carboxylic acid ethyl ester | HCID 67231190 | 20% |
Reaction Steps
Potassium carbonate (2.6 g, 18.7 mmol) and 1-iodopropane (669.7 μL, 6.9 mmol) were added to 2-(4-Bromobenzyl)-1H-imidazole-4-carboxylic acid ethyl ester (1.9 g, 6.2 mmol) dissolved in DMF (40 mL, 500 mmol). The mixture was heated at 60° C. for 5 hours. The mixture was cooled and then diluted with EtOAc (100 mL), washed with water and saturated aqueous NaCl (100 mL each), dried over MgSO4, filtered and concentrated. The mixture was purified by column chromatography (20-60% EtOAc in Hexanes) to yield the desired product, 2-(4-bromobenzyl)-1-propyl-1H-imidazole-4-carboxylic acid ethyl ester (736 mg, 33.6% yield), and its regioisomer, 2-(4-bromobenzyl)-3-propyl-3H-imidazole-4-carboxylic acid ethyl ester (500 mg, 20% yield). The structures were confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865755B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1607e973d712419f9db01b850d09dcc4 |
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| Source note | uspto-grants-2014_10 |
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