The Lithium–Halogen Exchange Reaction in Process Chemistry

Author(s):  
William Bailey ◽  
Terry Rathman
Molbank ◽  
10.3390/m1289 ◽  
2021 ◽  
Vol 2021 (4) ◽  
pp. M1289
Author(s):  
Sukanta Bar

5-propyl-2-((trityloxy)methyl)thiophene-3-carbaldehyde was synthesized by using the concept of chemo- and regioselective Br/Li exchange reaction from 3-bromo-5-propyl-2-((trityloxy)methyl)thiophene. This is a five-step protocol starting from thiophene with an overall yield of 33%. These lithium/halogen exchange reactions were carried out at −78 °C to rt over the period of 1 to 18 h depending on the reactivity of electrophiles.


2019 ◽  
Vol 58 (4) ◽  
pp. 2618-2626 ◽  
Author(s):  
Adharsh Raghavan ◽  
Brandon L. Mash ◽  
Tong Ren

1974 ◽  
Vol 29 (3-4) ◽  
pp. 206-208 ◽  
Author(s):  
Manfred Fild ◽  
Thomas Stankiewicz

The thiophosphonic and thiophosphinic halides, C6F5P(S)X2, (C6F5)2P(S)X, and R(C6F5)P(S)X (X = F, Cl, Br, and R = CH3, C2H5, tert-C4H9, C6H5) have been prepared, a) by addition of sulfur to the phosphorus(III) derivatives, b) by the reaction of chlorophosphoranes with H2S, and c) by halogen exchange reaction. The 31P- and 11F NMR data are discussed.


ChemInform ◽  
2010 ◽  
Vol 30 (28) ◽  
pp. no-no
Author(s):  
Bernard Boyer ◽  
El Mehdi Keramane ◽  
Severine Arpin ◽  
Jean-Louis Montero ◽  
Jean-Pierre Roque

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