Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2,6-DIIODO-4-NITROANILINE

2,6-DIIODO-4-NITROANILINE synthesis

10synthesis methods
-

Yield: 92%

Reaction Conditions:

with N-iodo-succinimide in water;acetonitrile at 25 - 30; for 0.25 h;

Steps:

General procedure for the diiodination reaction
To a solution of 4-nitroaniline, 1a (1.0 g, 7.2 mmol) and 0.01 mL water, sulfated polyborate (0.025 g, 2.5 wt%) in 7 mL anhyd. MeCN in a round bottom flask was added NIS solution (3.26 g, 14.4 mmol in 4.0 mL anhyd. MeCN) dropwise. The reaction mixture was stirred for 15 minutes at 25-30 °C, monitored by GC. After completion of the reaction, MeCN was distilled under vacuum at 40-45 °C. The residue was treated with 10 mL each of MDC and water, stirred for the mixture for 10-15 minutes; MDC layer was separated, washed with 1% sodium thiosulphate, dried over sodium sulfate, and evaporated under vacuum to obtain 2,6-diiodo-4-nitroaniline, 3a, 2.8 g (92% yield, 99% purity) as yellow crystalline solid. m.p. 250-252 °C (lit.51 105-109 °C); 1H NMR (400 MHz, DMSO-d6) δ 8.40 (s, 2H), 6.30 (s, 2H); C6H4I2N2O2; 389.92; GC-MS m/z 390.0. All the products of diiodination were identified by 1H NMR and GC-MS or LC-MS.

References:

Chaturbhuj, Ganesh;Ganwir, Prerna;Misal, Balu;Palav, Amey [Tetrahedron Letters,2021,vol. 74,art. no. 153154] Location in patent:supporting information

2,6-DIIODO-4-NITROANILINE Related Search: