HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622438Generated: October 25, 2026
Hydrochloric Acid → 4-Bromo-2,6-dinitroaniline
https://huagongshe.com/reaction/1622438
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromo-4,6-dinitroaniline | HCID 15752 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-2,6-dinitroaniline | HCID 3746608 | 97% |
Reaction Steps
A mixture of sodium sulfide nonahydrate (96 g, 400 mmol) and sulfur (12.8 g, 400 mmol) in a mixture of 400 mL of water and 100 mL of ethanol was heated at reflux under nitrogen for 1 h. The solution was added to a stirred suspension of 2-bromo-4,6-dinitrobenzenamine (104.8 g, 400 mmol) and ammonium chloride (20.8 g, 400 mmol) in a mixture of 400 mL of water and 700 mL of ethanol. The mixture was stirred at 65° C. for 30 min. Then 400 mL of 2N NaOH solution was added dropwise during a period of 30 min and the mixture was then stirred for a further 15 minutes at 65° C. After cooling, the mixture was poured onto a mixture of 2N HCl (400 mL), 1 kg ice and 1 L of water, stirred for 15 min to complete the reaction and extracted with ethyl acetate (1 L×3). The combined organic layers were dried over sodium sulphate and evaporated to give the crude product (90 g, 97%) as a rust-colored solid, which was used for the next step without further purification; LC/MS: MS (ES+) m/e 232 [M+H]+; 1H NMR (300 MHz, DMSO-d6) δ ppm 5.48 (s, 2H), 6.07 (s, 2H), 7.39 (d, J=2.7 Hz, 1H), 7.64 (d, J=2.7 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778937B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ec40050bfb7c43a58c9a5ef6177975fa |
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| Source note | uspto-grants-2014_07 |
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