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A new method for preparing 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds

A technology for organic phosphonates and compounds is applied in the new field of preparing 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds, which can solve the problem of harsh reaction conditions and difficult recycling. , the difficulty of synthesis technology, etc., to achieve the effect of mild and easy control of the reaction process, good industrial application prospects, and cheap and easy-to-obtain catalysts

Active Publication Date: 2021-09-07
HUNAN INSTITUTE OF SCIENCE AND TECHNOLOGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Or utilize but, above-mentioned method generally all adopts to air-sensitive reagent (P (O)-H compound, carbon tetrachloride etc.) and expensive transition metal catalyst (palladium, silver, rhodium, ruthenium etc.), and also exists The experimental steps are cumbersome, the catalyst is expensive and difficult to recycle, the reaction conditions are harsh, the substrate applicability is crossed, the yield is low, and the pollution to the environment is relatively large.
[0004] So far, there are still several problems in the efficient synthesis of organic phosphonate compounds, such as the quality of raw materials, the safety of production, and the stability and purity of products, and the synthesis technology is relatively difficult.

Method used

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  • A new method for preparing 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Bromide 109 mg (0.5 mmol) of diphenylphosphoric acid, 215 mg (0.5 mmol) of diphenyl trifluoromethanesulfonic acid periodate, 0.5 mmol of triethylamine and 7.2 mg (0.05 mmol) Cuprous, add 2.0 mL organic solvent (toluene, tetrahydrofuran, dichloromethane, dichloroethane, N,N -dimethylformamide, 1,4-dioxane, acetone, ethyl acetate, acetonitrile), at 100 o C stirred the reaction for 12 hours. Through GC detection and analysis, when tetrahydrofuran was used as the reaction solvent, the yield of the coupling reaction was 86%.

Embodiment 2

[0028] 109 mg (0.5 mmol) of diphenylphosphoric acid, 215 mg (0.5 mmol) of diphenyltrifluoromethanesulfonic acid periodate, 0.5 mmol of base (diisopropylethylamine, 1,8-di Azabicycloundec-7-ene, N,N - Dimethylaniline, N,N-Diethylaniline, N,N -Dimethylbenzylamine, triethylamine, potassium carbonate, sodium carbonate, potassium phosphate, potassium hydroxide, sodium hydroxide or cesium carbonate) and 7.2 mg (0.05 mmol) cuprous bromide, add 2.0 mL tetrahydrofuran, at 100 o C stirred the reaction for 12 hours. By GC detection analysis, when triethylamine is used as the base, the yield of the coupling reaction is 86%.

Embodiment 3

[0030] 109 mg (0.5 mmol) of diphenylphosphoric acid, 215 mg (0.5 mmol) of biphenyltrifluoromethanesulfonic acid periodate, 0.5 mmol of triethylamine and 0.05 mmol of copper salt (cuprous chloride , cuprous bromide, cuprous iodide, copper oxide, cuprous oxide, copper powder, copper chloride, copper bromide, copper acetate, copper trifluoromethanesulfonate, copper sulfate), add 2.0 mL tetrahydrofuran, at 100 o C stirred the reaction for 12 hours. By GC detection and analysis, when cuprous iodide is used as a catalyst, the yield of the coupling reaction is 92%.

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Abstract

The invention provides a new method for efficiently and highly selectively synthesizing 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds containing different functional groups, which uses cheap transition metal copper The salt is used as a catalyst, and the compound containing P(O)-OH and bisaryltrifluoromethanesulfonic acid periodiodium salt is used as a reaction substrate, and an organic solvent and a base are added to the reaction system. The advantages of the method are: the catalyst is cheap and easy to obtain; the substrate has high applicability; the reaction conditions are mild, safe and reliable; the selectivity of the obtained target product is close to 100%, and the yield is as high as more than 90%. The method solves the shortcomings of the traditional synthesis of 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds, such as poor reaction selectivity, cumbersome reaction steps, low yield, and the need to use environmentally harmful reagents. , has good industrial application prospects. The present invention also provides corresponding 2'-iodo[1,1'-biaryl]-2-organophosphonate derivatives substituted with different functional groups.

Description

technical field [0001] The invention relates to the field of catalytic synthesis of 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds, in particular to a copper-catalyzed P(O)-OH compound A new method for preparing 2'-iodo[1,1'-biaryl]-2-organophosphonate compounds through efficient cross-coupling reaction of aryl trifluoromethanesulfonic acid periodide salts. Background technique [0002] 2'-Halo[1,1'-biaryl]-2-organophosphonate compounds are an important class of organic compounds and organic intermediate building blocks in organic synthesis. This type of compound has good catalytic activity, optical activity and biological activity. In particular, iodo compounds, due to the high reactivity of iodide ions, can be selectively modified for the above compounds, making them widely used in biology, medicine, optically active materials, and asymmetric catalytic synthesis. In addition, phosphorus and organophosphorus compounds are indispensable in life, such as ADP, ATP, RNA, ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07F9/40
CPCC07F9/4021C07F9/4084
Inventor 熊碧权王刚唐课文刘宇许卫凤
Owner HUNAN INSTITUTE OF SCIENCE AND TECHNOLOGY
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