Ammonium Nitrate as a Catalyst in Organic Synthesis.

Pink crystals 0.178 g, 88% yield; mp 282˚C - 283˚C. IR (KBr pellet): 3422 (NH), 3015 (arom. CH), 2935 (aliph. CH), 1660 (C=N) cm–1. 1H NMR (DMSO-d6, 400 MHz): 12.66 (s, 1H), 12.23 (s, 1H), 9.15 (s, 1H), 8.08 (s, 1H), 2.35 (s, 3H), 2.30 (s, 3H). Anal. Calcd. for C9H10N6 (204.23): C, 52.93%; H, 5.92%; N, 41.15%. Found: C, 52.89%; H, 5.91%; N, 41.23%.

ethylammonium nitrate (CHEBI:63882) - EMBL-EBI

CAS No.20748-72-5,(2-Hydroxyethyl)ammonium nitrate …

Ethylammonium nitrate synthesis essay - brasserie …

[28] J. S. Yadav, B. V. S. Reddy, K. B. Reddy, K. S. Raj and A. R. Prasad, “Ultrasound-Accelerated Synthesis of 3,4- Dihydropyrimidine-2(1H)-Ones with Ceric Ammonium Nitrate,” Journal of the Chemical Society, Perkin Transaction 1, pp. 1939-1941.

Ethylammonium nitrate synthesis essay

[27] S. C. Roy and B. A. Banergie, “A Mild and Efficient Method for the Chemoselective Synthesis of Acylas from Aldehydes and Their Deprotections Catalysed by Ceric Ammonium Nitrate,” Synlett, Vol. 2002, No. 10, 2002, pp. 1677-1678.

Synthesis of iron (III) nitrate

[11] A. V. Tenkovvtsev, A. V. Yakimanski, M. M. Dudkina, V. V. Lukoshkin, H. Komber, L. Haussler and F. Bohme, “Ionic Complexes of Bis (Hydroxyarylidine) Alkanones with Strong Polymeric Bases as a New Class of ThirdOrder Nonlinear Optical Chromophors,” Macromolecules, Vol. 34, No. 20, 2001, pp. 7100-7107.

(benzyl tri ethyl ammonium chloride) ..

To a stirred mixture of each of aromatic or heteroaromatic amines 1a-f (20 mmol), triethylorthoformate (10 mmol) in water (20 mL) was added cerium (IV) ammonium nitrate (10 mol%). The reaction mixture was stirred at room temperature (27˚C) for 10 - 40 minutes. For liquid amines a solid was formed, while for solid amines, they dissolved in the reaction medium and then resolidified forming the final product. The resulting solid was collected by filtration and recrystallized from ethanol to afford analytically pure samples 3a-h. Compounds 3a-f have been described previously [31-37] and were found identical with our samples synthesized by our protocol.

Ionic Liquid Based Systems for Aromatic Nitration

and and and and and and (2012)Efficient, rapid synthesis of bis(indolyl)methane using ethyl ammonium nitrate as an ionic liquid. RSC Advances, 02. pp. 3525-3529.

Tetramethyl ammonium nitrate CAS NO.1941-24-8EINECS ..

[23] A.S. Ripak, D. D. Diaz, K. P. Sharpless and M. G. Finn, “Expanded Chemistry of Formamidine Ureas,” Organic Letters, Vol. 6, No. 1, 2004, pp. 43-46.


A simple and rapid protocol has been developed for an efficient synthesis of bis(indolyl) methane in excellent yields using ethyl ammonium nitrate (EAN) as reusable ionic liquid at room temperature. The protocol involves an electrophilic substitution reaction of indoles with several aldehydes.

Vinyl iodide synthesis by iodination or substitution

[31] K. U. Sadek, F. Al-Qalaf, M. M. Abdelkhalik and M. H. Elnagdi, “ Cerium (IV) Ammonium Nitrate as an Efficient Lewis Acid for the One-pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-Ones and Their Corresponding 2- (1H)-Thiones,” Journal of Heterocyclic Chemistry, Vol. 47, No. 2, 2010, pp. 284-286.