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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082043Generated: November 1, 2026

4-Phenoxyphenol → HCID 14402693, compound

https://huagongshe.com/reaction/2082043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxyphenolHCID 13254—
ReactantSodium hydrideHCID 24758—
Reactant1H-Imidazole, 4,5-dichloro-1-(chloromethyl)-HCID 14402692—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14402693HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187182
Source datasetuspto-grants-1993_02
ORD IDord-94fb8bfe661f4ad39e7871f93d389f00
Source noteuspto-grants-1993_02