Method for preparing 2-iodoheterocyclic aryl ether at room temperature

US12371413B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12371413-B2
Application numberUS-202118012586-A
CountryUS
Kind codeB2
Filing dateFeb 22, 2021
Priority dateFeb 22, 2021
Publication dateJul 29, 2025
Grant dateJul 29, 2025

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  1. Title

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  2. Abstract

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Abstract

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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.

First claim

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.

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What does patent US12371413B2 cover?
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 …
Who is the assignee on this patent?
Univ Soochow
What technology area does this patent fall under?
Primary CPC classification C07D333/32. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 29 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).