![](/CAS/GIF/58580-07-7.gif)
2-amino-5-bromo-3-nitrobenzoic acid synthesis
- Product Name:2-amino-5-bromo-3-nitrobenzoic acid
- CAS Number:58580-07-7
- Molecular formula:C7H5BrN2O4
- Molecular Weight:261.03
![5-bromo-7-nitroindoline-2,3-dione](/CAS/20180703/GIF/49764-59-2.gif)
49764-59-2
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![2-amino-5-bromo-3-nitrobenzoic acid](/CAS/GIF/58580-07-7.gif)
58580-07-7
42 suppliers
$50.00/250mg
Yield:58580-07-7 96%
Reaction Conditions:
with dihydrogen peroxide;sodium hydroxide in water at 0 - 20; for 4 h;
Steps:
2 Preparation 2: 2-amino-5-bromo-3-nitro-benzoic acid
To a stirred solution of 5-bromo-7-nitro-1H-indole-2,3-dione (5.5 g, 20.3 mmol) in an aq.solution of 2N NaOH (23.2 mL) was added a 50% solution of H202 in water (4.96 mL) slowly at 0°C. Then allowed to warm to room temperature and stirred for 4 h. The progress of the reaction was monitored by TLC and the reaction mixture was diluted with water and acidified with citric acid to pH-4. The yellow solid formed was filtered and dried under vacuum to get the title compound (5.0 g, 96.0%). ‘H NMR (400 MHz, DMSO-d6): ? 8.84 (bs, 2H), 8.59 (s, 1H), 8.37 (s, 1H).
References:
WO2018/154088,2018,A1 Location in patent:Paragraph 0144
![2-Amino-3-nitrobenzoic acid](/CAS/GIF/606-18-8.gif)
606-18-8
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$9.00/1g
![2-amino-5-bromo-3-nitrobenzoic acid](/CAS/GIF/58580-07-7.gif)
58580-07-7
42 suppliers
$50.00/250mg
![3-Nitrophthalic acid](/CAS/GIF/603-11-2.gif)
603-11-2
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$15.00/25g
![2-amino-5-bromo-3-nitrobenzoic acid](/CAS/GIF/58580-07-7.gif)
58580-07-7
42 suppliers
$50.00/250mg
![3-Nitrophthalic anhydride](/CAS/GIF/641-70-3.gif)
641-70-3
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$6.00/5g
![2-amino-5-bromo-3-nitrobenzoic acid](/CAS/GIF/58580-07-7.gif)
58580-07-7
42 suppliers
$50.00/250mg
![5-Bromoisatin](/CAS/GIF/87-48-9.gif)
87-48-9
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$10.00/5g
![2-amino-5-bromo-3-nitrobenzoic acid](/CAS/GIF/58580-07-7.gif)
58580-07-7
42 suppliers
$50.00/250mg