Related Products of 2674-34-2, These common heterocyclic compound, 2674-34-2, name is 1,4-Dibromo-2,5-dimethoxybenzene, 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.
Boronate ester 10 (1.00g, 3.15mmol), dibromoarene 11 (310mg, 1.05mmol), and K2CO3 (1.88g, 13.6mmol) in toluene (40mL), EtOH (10mL), and H2O (5mL) was sparged with Ar for 1h. Pd(PPh3)4 (120mg, 0.10mmol) was added, the mixture was sparged for an addition 15min with Ar, and then refluxed for 16h. The reaction mixture was allowed to cool to rt and 30mL of H2O was added to the reaction. The reaction mixture was extracted with Et2O (3×30mL). The combined organics were dried with Na2SO4 and the solvent removed under vacuum. The product was isolated with column chromatography to afford a white/light yellow solid (506mg, 93%), mp 151-154C. 1H NMR (CDCl3): delta 7.83 (d, J=8.5Hz, 2H), 7.45-7.44 (m, 4H), 6.84 (s, 2H), 3.71 (s, 12H), 1.38 (s, 18H). 13C NMR (CDCl3): delta 168.7, 154.9, 150.3, 138.2, 130.6, 129.3, 128.9, 128.4, 124.3, 113.0, 56.0, 51.6, 35.0, 31.18. FTIR (cm-1): 1725.25. UV-vis (CH2Cl2) lowest E abs lambdamax [nm] ( [M-1cm-1]): 326 (10,609). Em. (CH2Cl2) lambdamax [nm]: 409. Anal. Calcd for C32H38O6: C, 74.11; H, 7.39. Found: C, 73.98; H, 7.38.
Statistics shows that 1,4-Dibromo-2,5-dimethoxybenzene is playing an increasingly important role. we look forward to future research findings about 2674-34-2.
Article; Dressler, Justin J.; Miller, Sarah A.; Meeuwsen, Brian T.; Riel, Asia Marie S.; Dahl, Bart J.; Tetrahedron; vol. 71; 2; (2015); p. 283 – 292;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem