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ChemicalBook CAS DataBase List 4-ISOPROPYL-OMEGA-NITROSTYRENE

4-ISOPROPYL-OMEGA-NITROSTYRENE synthesis

3synthesis methods
-

Yield:42139-37-7 72%

Reaction Conditions:

with copper(II) nitrate trihydrate in water;acetonitrile at 130; for 12 h;

Steps:

14 Example-14

Add 0.3 mmol of isopropyl cinnamaldehyde and 0.45 mmol of copper nitrate trihydrate to a 15 mL pressure tube, and then add 3 mL of a mixture of acetonitrile and water (V (acetonitrile): V (water) = 100:1) as solvent . Next, stirring was performed at 130° C. (magnetic stirring for 12 hours). Then, two shots of column chromatography silica gel (100-200 mesh) was added to the reaction solution, and the solvent was removed by distillation under reduced pressure. The residue was separated by column chromatography. Using a mixture of V (petroleum ether):V (ethyl acetate) = 20:1 as eluent, the eluent containing the target product was collected, and the solvent was distilled off to obtain pure product. The amount of pure product was: 0.216 mmol The material was a yellow solid, chemical name 2-nitro-p-isopropylstyrene, yield 72%.

References:

CN107641086,2018,A Location in patent:Paragraph 0078-0080

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