HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279443Generated: October 30, 2026
Imidazole → 1-[2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl]imidazole
https://huagongshe.com/reaction/279443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl chloride | HCID 54432646 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[2-(3-Chlorophenoxymethyl)-alpha-methoxyiminobenzyl]imidazole | HCID 53995437 | 65.3% |
Reaction Steps
Dimethylformamide (3 ml) and 60% sodium hydride (0.16 g, 3.9 mmol) were added to imidazole (0.27 g, 3.9 mmol), and the mixture was stirred at room temperature for 10 minutes. Then, 2-(3-chlorophenoxymethyl)-α-methoxyiminobenzyl chloride (0.40 g, 1.3 mmol) was added, and the mixture was stirred at 110° C. for 2 hours. After completion of the reaction, ether (100 ml) was added, and the mixture was washed with brine (80 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 1-[2-(3-chlorophenoxymethyl)-α-methoxyiminobenzyl]imidazole (0.29 g, 65.3%) as colorless crystals. mp. 96.5-97.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06362212B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-83aa2cd0f955485f870949d6486719a2 |
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| Source note | uspto-grants-2002_03 |
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