HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439457Generated: October 30, 2026
Sodium Hydroxide → 4,5-Dibromobenzene-1,2-diamine
https://huagongshe.com/reaction/439457
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4,5-Dibromo-2-nitroaniline | HCID 12711027 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4,5-Dibromobenzene-1,2-diamine | HCID 12196944 | 97% |
Reaction Steps
To a solution of 4,5-dibromo-2-nitroaniline (3.35 g, 11.32 mmol) in EtOAc (150 mL) was added stannous chloride dihydrate (12.8 g, 56.74 mmol), the mixture was stirred at 75° C. for 16 h, then allowed to cool to room temperature and poured into ice-water (about 150 mL). To the mixture was added 1N aq NaOH with vigorous stirring to take the pH to 9 (pH paper). The resulting thick yellow white emulsion was extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with brine (2×50 mL), dried (over Na2SO4) and evaporated to dryness. The residual solid was dried under 1 mmHg at 40° C. for 14 h giving 2.92 g (97%) of 4,5-dibromo-1,2-phenylenediamine as a yellowish powder. Mp 149°-50° C. IR (KBr) 3400, 1623, 1489, 1394, 1271, 868 cm-1. 1H NMR (DMSO-d6) 6.754 (s, 2H), 4.867 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514680 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-71974282c0cc43409a9c98be9271fbab |
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| Source note | uspto-grants-1996_05 |
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