Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18437850 | HCID 18437850 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18437798 | HCID 18437798 | — |
Reaction Steps
A solution of 1 mmol of 3,4-dichloroimidazole in anhydrous DMF (5 mL) is treated with sodium hydride (1.05 mmol) at 0° C. under nitrogen with magnetic stirring. After 30 min., 2-chloroethyl methyl ether (1 mmol) is added and the reaction mixture is warmed to 60° C. for 2 h. The reaction mixture is cooled, portioned between water and ethyl acetate. The organic layer is separated, washed with water, brine and dried over sodium sulfate. The reaction mixture is filtered, evaporated and purified by chromatography on silica gel to obtain 1-methoxyethyl-3,4-dichloroimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186734B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-949e67d40e7f4bac8c1bcde4877a1c70 |
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| Source note | uspto-grants-2007_03 |
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