![](/CAS/GIF/38791-62-7.gif)
4-PHENOXYPHTHALONITRILE synthesis
- Product Name:4-PHENOXYPHTHALONITRILE
- CAS Number:38791-62-7
- Molecular formula:C14H8N2O
- Molecular Weight:220.23
![4-Nitrophthalonitrile](/CAS/GIF/31643-49-9.gif)
31643-49-9
436 suppliers
$6.00/5g
![Phenol](/CAS/20180808/GIF/108-95-2.gif)
108-95-2
725 suppliers
$14.00/25g
![4-PHENOXYPHTHALONITRILE](/CAS/GIF/38791-62-7.gif)
38791-62-7
68 suppliers
$22.00/250mg
Yield: 86.4%
Reaction Conditions:
with sodium hydride in tetrahydrofuran for 8 h;Inert atmosphere;Reflux;
Steps:
Synthesis of 2,3,9,10,16,17,23,24-octa substituted phthalocyanine (2a)
To NaH (0.15 g) and phenol, (0.353 g,0.0375 mol) in THF (15 mL) was added and 4-nitrophthalonitrile(0.50 g, 0.0028 mol), in THF (15 mL) and refluxed for 8 h. The resulting 1,2-diisocyano-4-phenoxybenzene (8) was filtrated and the solid washed with ethyl acetate and both the filtrate and the washing were mixed and evaporated under reduced pressure (Scheme-II). The resulting white precipitate was purified by flash column chromatography using solvent system, ethyl acetate:hexane (1:4). Yield = 0.737 g, % Yield =86.4, Rf = 0.36 (ethyl acetate:hexane, 1:4). 1H NMR (300 MHz, CDCl3) δ 0.90 (s, 2H), 3.46 (m, 5H,CH) 7.07 (m, 3H, ArH), 13C NMR (300 MHz, CDCl3) δ 71.01,117.45, 119.69, 119.92, 126.95, 127.34, 134.43, 135.20.
References:
Isabirye, David A.;Seheri, Naledi H.;Aiyelabola, Temitayo O. [Asian Journal of Chemistry,2017,vol. 29,# 3,p. 489 - 495]
![4-Nitrophthalonitrile](/CAS/GIF/31643-49-9.gif)
31643-49-9
436 suppliers
$6.00/5g
![Sodium benzenolate](/CAS/GIF/139-02-6.gif)
139-02-6
123 suppliers
$34.00/5g
![4-PHENOXYPHTHALONITRILE](/CAS/GIF/38791-62-7.gif)
38791-62-7
68 suppliers
$22.00/250mg