HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967982Generated: October 30, 2026
Iodoethane → 1-ethyl-1H-imidazole-2-carbaldehyde
https://huagongshe.com/reaction/1967982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-ethyl-1H-imidazole-2-carbaldehyde | HCID 11062377 | 84% |
Reaction Steps
To a suspension of 1H-imidazole-2-carbaldehyde (480 mg, 5 mmol) and potassium carbonate (936 mg, 6 mmol) in N,N-dimethylformamide (7 mL) was added iodoethane (829 mg, 6 mmol) and the mixture was heated at 50° C. for 5 hrs. Solvent was removed under reduced pressure. The residue was partitioned between water (30 mL) and ethyl acetate (30 mL). The aqueous layer was extracted with ethyl acetate (20 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give 1-ethyl-1H-imidazole-2-carbaldehyde as light yellow oil (520 mg, yield 84%). 1H NMR (400 MHz, CDCl3) δ (ppm): 1.42-1.46 (t, J=7.2 Hz, 3H), 4.42-4.47 (q, 2H), 7.19 (s, 1H), 7.29 (s, 1H), 9.82 (s, 1H). LC-MS (ESI) m/z: 125 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420650B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-b991f40bab314c948700a07c0ba92eb6 |
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| Source note | uspto-grants-2013_04 |
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