Macromolecular compound
US-2016372675-A1 · Dec 22, 2016 · US
US12371413B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12371413-B2 |
| Application number | US-202118012586-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2021 |
| Priority date | Feb 22, 2021 |
| Publication date | Jul 29, 2025 |
| Grant date | Jul 29, 2025 |
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Disclosed is a method for preparing a 2-iodoheterocyclic aryl ether at room temperature, including adding an alkali metal hydride and a phenol to a solvent, then adding a diiodoheterocyclic aromatic hydrocarbon, and performing a reaction at 0-100° C., so as to obtain a 2-iodoheterocyclic aryl ether product. In the coupling process of the present invention, no transition metal catalyst needs to be added, and no metal pollution will be caused to the product. The product of the present invention can be used as an organic synthesis raw material for a further reaction, and can also be used as an additive flame retardant reagent to improve the flame retardant performance of plastics.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a 2-iodo-heterocyclic aromatic ether at room temperature comprising following steps: reacting a 2-iodo-heterocyclic aromatic hydrocarbon with a phenol in the presence of an alkali metal hydride to obtain the 2-iodo-heterocyclic aromatic ether, wherein the 2-iodo-heterocyclic aromatic ether is and Ar 2 is benzene, naphthalene, pyridine, quinoline, pyrimidine, or thiophene. 2. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 1 , comprising adding the alkali metal hydride and the phenol into a solvent, then adding the 2-iodo-heterocyclic aromatic hydrocarbon to obtain the 2-iodo-heterocyclic aromatic ether. 3. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 2 , wherein the solvent is one or more selected from the group consisting of DMF, DMA, THF, 2-MeTHF, DME, MTBE, diethyl ether, DMSO, NMP, and toluene. 4. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 1 , wherein the alkali metal hydride is sodium hydride, potassium hydride or calcium hydride; the phenol is unsubstituted phenol, a substituted phenol or a heterocyclic phenol. 5. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 1 , wherein a mole ratio of the phenol to the 2-iodo-heterocyclic aromatic hydrocarbon to the alkali metal hydride is 1:(0.1-10):(1.2-10). 6. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 5 , wherein a mole ratio of the phenol to the 2-iodo-heterocyclic aromatic hydrocarbon to the alkali metal hydride is 1:(0.5-5):(1.5-5). 7. The method for preparing the 2-iodo-heterocyclic aromatic ether at room temperature according to claim 1 , wherein a reaction temperature is 10-50° C.; a reaction time is 0.2-10 hours.
Halogen atoms · CPC title
Oxygen atoms · CPC title
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