Synthetic Route of 38791-62-7, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 38791-62-7, name is 4-Phenoxyphthalonitrile belongs to nitriles-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.
General procedure: 1,2-Diisocyano-4-phenoxy benzene (8) (0.300 g, 1.36 ×10-3 mol) and phenol (0.356 g, 0.0375 mol) in THF was refluxed. The resultant product (9), 1,2-diisocyano-3,4-diphenoxy benzene,(0.300 g, 1.36 × 10-3 mol) was refluxed in 1-pentanol (14 mL)and 1 mol 1,8-diazabicyclo[5.4.0]-undec-7-ene (0.21 g, 1.36× 10-3 mol) for 16 h. Methanol (20 mL) was there after added and the precipitate (2a) filtered off, Soxhlet extracted with methanol and acetone and dried at 60 C. Yield = 0.294 g and yield (%) 43, Rf = 0.23 (ethyl acetate:hexane, 3:8). (KBr, numax,cm-1): 3620 (N-H), 2848 (C-H) aromatic, 1685 (C=C), 1163(C-H), 743 (C-H). UV-visible lambdamax (nm): 337, 606, 640, 661,702. 1H NMR (300 MHz, CDCl3) delta 2.01 (s, 2H, NH), 3.66 (m,4H, CH), 6.99 (m, 4H, ArH), 7.23 (m, 4H, ArH), 7.50 (m, 4H,ArH) 8.04 (m, 4H, ArH), 8.99 (m, 4H, ArH), 9.23 (m, 4H,ArH), 13C NMR (300 MHz, CDCl3) delta 71.01, 76.57, 76.99,77.41, 117.45, 119.69, 119.92, 126.95, 127.48, 127.63, 128.53,128.85, 128.94, 134.43, 135.20. Anal. calcd. C, 76.21; H, 4.19;N, 9.03. Found: C, 76.21; H, 4.18; N, 9.11.
In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 4-Phenoxyphthalonitrile, other downstream synthetic routes, hurry up and to see.
Reference:
Article; Isabirye, David A.; Seheri, Naledi H.; Aiyelabola, Temitayo O.; Asian Journal of Chemistry; vol. 29; 3; (2017); p. 489 – 495;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts