HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761854Generated: October 28, 2026
Hydrogen Bromide → Benzene, 1,2,3-tribromo-5-nitro-
https://huagongshe.com/reaction/1761854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2,6-Dibromo-4-nitroaniline | HCID 13231 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Benzene, 1,2,3-tribromo-5-nitro- | HCID 640602 | — |
Reaction Steps
At 20° C., with stirring and cooling with ice, a solution of 2,6-dibromo-4-nitro-aniline (47.2 g) in acetic acid (1.6 liters) is slowly poured into a solution of sodium nitrite (12 g) in concentrated sulphuric acid (85 ml). Then, the mixture is stirred for 20 minutes at ambient temperature. The solution thus prepared is then slowly added with stirring and cooling with ice to a solution of copper (I) bromide (12.8 g) in 63% hydrobromic acid (40 ml)/. After it has all been added the mixture is stirred for a further 30 minutes. It is diluted with water, the precipitate is filtered off and washed with water. This crude product is recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04829058 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-b3962a5c67d4484f818ad07fa756ae8c |
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| Source note | uspto-grants-1989_05 |
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