HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249357Generated: October 29, 2026
4-Phenoxyphenol → HCID 14402693, compound
https://huagongshe.com/reaction/249357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-Imidazole, 4,5-dichloro-1-(chloromethyl)- | HCID 14402692 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14402693 | HCID 14402693 | — |
Reaction Steps
9.3 g of 4-phenoxyphenol is dissolved in 60 ml of anhydrous dimethylformamide. 1.58 g of 80% strength sodium hydride is added, and the mixture is heated at 60° C. until no more hydrogen evolves (about 1 hour). A solution of 9.28 g of N-(1-chloromethyl)-4,5-dichloroimidazole in 30 ml of dimethylformamide is then dripped in. The mixture is stirred overnight at room temperature, after which it is poured into 500 ml of water, followed by extraction three times with methyl tert-butyl ether. The combined organic phases are washed three times with water, dried over sodium sulfate, and freed from solvent under reduced pressure. The solid residue is recrystallized from n-pentane/ether (6:1) to give N-[(p-phenoxyphenoxy)-methyl]-4,5-dichloroimidazole, m.p.: 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214064 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-a30a3ee83f0a412cbb2dc1040ae65e4a |
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| Source note | uspto-grants-1993_05 |
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