HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388408Generated: November 1, 2026
2-Methylimidazole → 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde
https://huagongshe.com/reaction/1388408
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(3-Bromopropyl)-1-piperidinecarboxaldehyde | HCID 20239768 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde | HCID 20239782 | 88% |
Reaction Steps
A mixture of 2-methylimidazole (2 g, 0.025 M) and sodium hydride (1.2 g, 50% in mineral oil, 0.025 M) in dimethylformamide (20 ml) was stirred at room temperature for 1/2 hr. The reaction mixture was then heated at 50° C. and the solution of 4(3-bromopropyl)piperidine carboxaldehyde (4.6 g, 0.02 M) in dimethylformamide (20 ml) was added slowly. After completing the addition, the reaction was heated at 50° C. for 4 hrs and then solvent was removed in vacuo. Water (80 ml) was added to the residue and the mixture was extracted with methylene chloride. The combined extracts, dried over sodium sulfate, were stripped to dryness to yield an oil. The oil was purified on silica gel column, eluted with methanol chloroform (1:9 v/v) to give 4-[3-(2-methyl-1H-imidazol-1-yl)-propyl]-1-piperidinecarboxaldehyde (3.86 g, 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431653 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-2846eaa71cea4007a55a86030ff9be72 |
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| Source note | uspto-grants-1984_02 |
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