Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

2-(3,4-DIFLUOROPHENYL)PYRIDINE synthesis

4synthesis methods
-

Yield:387831-85-8 96.2%

Reaction Conditions:

with dmap;copper(II) ethylacetoacetate;C26H36NP;silver(I) acetate in propan-1-ol at 60; for 12 h;Reagent/catalyst;

Steps:

1 Example 1: 2-(3,4-Difluorophenyl)pyridine

To the appropriate amount of n-propanol in the reactor, 100 mmol of 3,4-difluorobenzoyl chloride, 100 mmol of n-butylamine, 5 mmol of copper(II) ethylacetoacetate, 5 mmol Ligand L1,100mmol dimethylaminopyridine 20mmol silver acetate and the mixture was stirred to warm to 60 , and stirring was continued at this temperature for 12 hours.
After the completion of the reaction, the reaction system was allowed to cool to room temperature, washed thoroughly with deionized water and the layers were separated. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography,The eluent used was a mixture of ethyl acetate and n-butanol, both the volume ratio of 1: 3, i.e., of formula (I), 2- (3,4-difluorophenyl) pyridine, yield 96.2%.

References:

CN104529879,2016,B Location in patent:Paragraph 0045; 0046; 0047; 0048; 0049; 0050; 0051