HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196971Generated: October 30, 2026
Imidazole → N-[(p-phenoxyphenoxy)-n-propyl]-imidazole
https://huagongshe.com/reaction/1196971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(3-Bromopropoxy)1-phenoxybenzene | HCID 11255243 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[(p-phenoxyphenoxy)-n-propyl]-imidazole | HCID 14402690 | 82.2% |
Reaction Steps
1.98 g of 80% strength sodium hydride is added in portions to a solution of 4.25 g of imidazole in 70 ml of dimethylformamide. Upon completion of hydrogen evolution the mixture is stirred for a further 3 hours at 60° C., after which a solution of 18.42 g of 3-[4-(phenoxy)-phenoxy]-1-bromopropane in 40 ml of dimethylformamide is added. The mixture is heated for 8 hours at 80° C. and then poured into 2.5 liters of ice water. The solid which separates out is filtered off in a desiccator, dried over calcium chloride and purified by filtration over silica gel. There is obtained 14.5 g (82%) of N-[(p-phenoxyphenoxy)-n-propyl]-imidazole; m.p.: 54.5°-55.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116860 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-b12ffcafeab74c35871ebc941b1a751a |
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| Source note | uspto-grants-1992_05 |
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