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ChemicalBook CAS DataBase List 3-BROMO-5-IODOANILINE

3-BROMO-5-IODOANILINE synthesis

5synthesis methods
861601-15-2 Synthesis
1-bromo-3-iodo-5-nitrobenzene

861601-15-2
62 suppliers
$49.00/1g

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Yield: 96%

Reaction Conditions:

with iron;acetic acid at 20; for 16 h;

Steps:

1.3
3-Bromo-5-iodoaniline.A mixture of 3-Bromo-5-iodonitrobenzene (4.21 g, 0.0128 mol) and iron powder (3.6g, 0.0642 mol) in glacial acetic acid (50 ml) was stirred at ambient temperature for 16 h. The reaction mixture was then filtered through a pad of celite and washed through with ethyl acetate. The filtrate was evaporated in vacuo to give a brown oil. This was re-dissolved in ethyl acetate, loaded onto a large pad of silica and eluted with ethyl acetate. The filtrate was evaporated in vacuo to afford 3-Bromo-5- iodoaniline as a brown solid (3.67g, 96%) which was used without further purification. 1H NMR (400MHz,δ,CDCI3): 3.72(2H,br s), 6.77(1 H,s), 6.95(1 H,s), 7.21(1 H,s).

References:

PROLYSIS LTD. WO2007/148093, 2007, A1 Location in patent:Page/Page column 14-15