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Application of dibromotriphenylphosphine
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Time :2021-12-09
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1 Application of dibromotriphenylphosphine


Dibromotriphenylphosphine is often used as a brominating agent in organic synthesis, and its structural formula is as follows:

二溴三苯基膦-图1.png

 

Dibromotriphenylphosphine was first used in the synthesis reaction in 1959 to prepare bromide and acid bromide from alcohol and carboxylic acid, and it was also used in the dehydration reaction of amides and oximes to nitriles. Now it has been used as a general reagent in many reactions.


Application 1: Alcohol Synthesis of Bromide

The reaction between dibromotriphenylphosphine and alcohol first generates alkoxytriphenylphosphine bromide intermediate, which reacts very quickly, and then the intermediate slowly decomposes into triphenylphosphine oxide and corresponding bromide. The by-product triphenoxyphosphine can be removed by distillation or beating, and the yield is relatively high.

An example of the reaction is shown in the figure below:

 

二溴三苯基膦-图2.png

 


Application 2: bromination reaction

Dibromotriphenylphosphine is also a good bromination reagent, which can replace bromine in many reactions and enhance the operability of the reaction.

An example of the reaction is shown in the figure below:

 

二溴三苯基膦-图3.png

 

 

 

Application 3: Synthesis of aryl bromide

The reaction of dibromotriphenylphosphine and phenol can prepare brominated aromatic compounds, but the reaction yield is low.

An example of the reaction is shown in the figure below:

二溴三苯基膦-图4.png

 

 

 

Application 4: The reaction of ring-opening of epoxides to form o-dibromo compounds

Epoxides and dibromotriphenylphosphine undergo ring-opening reactions in toluene to form o-dibromo compounds.

An example of the reaction is shown in the figure below:


二溴三苯基膦-图5.png

 

 

Application 5: Preparation of bromoalkenes by reacting with ketones

The reaction of dibromotriphenylphosphine and ketone compound to prepare brominated unsaturated compound has a higher yield.

An example of the reaction is shown in the figure below:


二溴三苯基膦-图6.png

 

The two-step total yield of the reaction can reach 54%.

 

Application 6: Reaction with carboxylic acid and acid anhydride to generate acid bromide

Acyl bromide can be prepared by reacting dibromotriphenylphosphine with carboxylic acid or acid anhydride, and the yield of this type of reaction is relatively high.

An example of the reaction is shown in the figure below:


二溴三苯基膦-图7.png

 

The reaction yield can reach 89%.

Application 7: Dehydration reaction of amides and oximes to nitriles

Dibromotriphenylphosphine can also be used as a dehydrating agent to dehydrate amides and oximes to form nitriles, and the reaction effect is very good.

An example of the reaction is shown in the figure below:

 

二溴三苯基膦-图8.png

 

 

In addition to the above applications, dibromotriphenylphosphine can also participate in the following reactions:


二溴三苯基膦-图9.png

 

references:

1. Jeffery, K.; Slayton, AWEJ Org. Chem., 1986, 51, 5490.

2. Chavan, SP; Kharul, RK; Kamat, SK; Kalkote, UR;Kale, RR Synth. Commun., 2005, 35, 987.

3. Menger, FM; Galloway, ALJ Am. Chem. Soc., 2004, 126, 15883.

4. Czarnik, AWJ Org. Chem., 1984, 49, 924.

5. Kamei, K.; Maeda, N.; Tatsuoka, T. Tetrahedron Lett., 2005, 46, 229.

6. Georgin, D.; Taran, F.; Mioskowski, C. Chem. Phys. Lipids., 2003, 125, 83.

7. Aizpurua, JM; Cossio, FP; Palomo, CJ Org. Chem., 1986, 51, 4941.

8. Pandey, MK; Bisai, A.; Singh, VK Tetrahedron Lett., 2004, 45, 9661.

9. Rocca, P.; Marsais, F.; Godard, A.; Queguiner, G.; Adams, L.;Alo, B. Tetrahedron Lett., 1995, 36, 7085.

10. "Modern Organic Synthetic Reagents - Properties, Preparation and Reaction", edited by Hu Yuefei and others

 

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