HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978039Generated: October 26, 2026
Dimethylformamide → 4-Chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazole
https://huagongshe.com/reaction/978039
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(4-Ethoxyphenoxy)benzyl chloride | HCID 13730380 | — |
| Reactant | HCID 178432150 | HCID 178432150 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazole | HCID 13730381 | 34.1% |
Reaction Steps
To a mixture of anhydrous N,N-dimethylforamide (10 ml) and sodium hydride (62% oil suspension; 0.071 g), 4-chloro-2-methylbenzimidazole (0.304 g) was added while stirring, and the stirring was continued at room temperature for 1 hour. The resultant mixture was cooled to 5°-10° C., and a solution of 4-(4-ethoxyphenoxy)benzyl chloride (0.400 g) in anhydrous N,N-dimethylformaide (10 ml) was dropwise added thereto in 30 minutes, followed by stirring at room temperature overnight. After completion of the reaction, the reaction mixture was poured into water (100 ml) and extracted with toluene (30 ml) two times. The toluene extract was washed with water, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove toluene. The residue was purified by silica gel column chromatography to give 4-chloro-1-[4-(4-ethoxyphenoxy)benzyl]-2-methylbenzimidazole (0.204 g) as a colorless liquid. nD26.5 1.6087.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663339 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-c19943473bb44129a190c8b13b394e5d |
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| Source note | uspto-grants-1987_05 |
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