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ChemicalBook CAS DataBase List 3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline
943320-48-7

3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline synthesis

2synthesis methods
54962-75-3 Synthesis
3-Amino-5-bromobenzotrifluoride

54962-75-3
299 suppliers
$5.00/1g

3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline

943320-48-7
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Yield:943320-48-7 63%

Reaction Conditions:

with copper(l) iodide;caesium carbonate in N,N-dimethyl-formamide at 20 - 130;Reagent/catalyst;Solvent;

Steps:

1.2; 2.2; 3.2; 4.2 Step 2: Preparation of 3-(1H-imidazol-1-yl)-5-trifluoromethylaniline

The 3-bromo-5-trifluorobenzylaniline (2g, 0.0084mol) prepared in step 1 was dissolved in 15mL solution of DMF. Add 2.5g of cesium carbonate (0.0076mol), imidazole (1.16g, 0.0235mol), cuprous iodide (0.16g, 0.00084mol), stir at room temperature for 10min, then heat the reaction system to 130 and stir for 16-20h, TLC monitors the reaction Complete, cool to room temperature, filter, add 15mL water to the filtrate, stir at room temperature for 30min, add ethyl acetate to extract 4 times (15mL*4) and wash the organic phase 4 times with water, separate the organic phase, dry and concentrate the organic phase to obtain 1.78g crude product. The crude product is purified by column chromatography, the eluent DCM:MeOH is 50:1-20:1 (gradient elution: DCM:MeOH is stirred evenly at a ratio of 50:1 to separate the less polar impurities, the elution process Using TLC monitoring in the medium, when the impurity disappears, the target product is separated evenly by stirring according to the ratio of 20:1) to obtain 1.2 g of 3-imidazol-1-yl-5-trifluoromethylaniline as a pale yellow solid, and the yield is 63%.

References:

CN112778207,2021,A Location in patent:Paragraph 0039; 0048; 0051-0055; 0058-0060; 0063-0065; 0068

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