HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194957Generated: November 2, 2026
Imidazole → 1H-Imidazole, 1-[2-(2-methoxyethoxy)ethyl]-
https://huagongshe.com/reaction/2194957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-3,6-dioxaheptane | HCID 123532 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1H-Imidazole, 1-[2-(2-methoxyethoxy)ethyl]- | HCID 54483278 | 70% |
Reaction Steps
Imidazole 1 g (0.015 mol) was dissolved in dry DMF 50 mL under argon atmosphere. After a NaH mineral oil dispersion (60%) 0.68 g (0.017 mol) was added, the mixture was heated at 80° C. for 70 min. After cooling to room temperature, 1-Bromo-2-(2-methoxyethoxy)-ethane (1), 2.75 g (0.015 mol), was added, then stirred overnight. The reaction was poured into water, extracted by CHCl3, washed by water, dried over Na2SO4, then dried (Rotavap) until an oily residue remained. The crude product was purified with silica gel flash column chromatography with an eluant of CHCl3: CH3OH=20:1. 1.69 g (70% yield) of the product (2) was obtained as a colorless oil. As an alternative to column chromatography, product (2) is purified by vacuum distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334377B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-2dce1d926f1a439bb55c3273b29a2623 |
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| Source note | uspto-grants-2012_12 |
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