Application of 1-Ethyl-4-iodobenzene

Statistics shows that 1-Ethyl-4-iodobenzene is playing an increasingly important role. we look forward to future research findings about 25309-64-2.

Electric Literature of 25309-64-2, These common heterocyclic compound, 25309-64-2, name is 1-Ethyl-4-iodobenzene, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

General procedure: To a large microwave tube (Biotage, 10-20 mL) equipped with a stir bar was added Pd(OAc)2(23.4 mg, 0.10 mmol, 10 mol %), S-1 (400 mg, 1.04 mmol, 1 equiv), cesium pivalate (731 mg,3.12 mmol, 3 equiv), aryl iodide (2-3 equiv) and anhydrous tert-amyl alcohol (9.6 mL). The capwas crimped and the vessel was flushed with nitrogen. The microwave tube was heated withfollowing parameters: 1 min pre-stirring, followed by a ramp (normal) to 180 C and held attemperature for 30 to 50 min. Hydrazine (500 muL of 35% aqueous) was added to the reaction andallowed to stir at 60 C for 1 hr or at room temperature overnight. The tert-amyl alcohol wasremoved en vacuo and the remaining residue dissolved with EtOAc, filtered through a plug ofcelite, and concentrated en vacuo. The crude reaction was purified via flash columnchromatography with EtOAc/Heptanes.

Statistics shows that 1-Ethyl-4-iodobenzene is playing an increasingly important role. we look forward to future research findings about 25309-64-2.