HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468098Generated: October 31, 2026
5-Chloro-2-nitroaniline → 5-Chloro-4-iodo-2-nitroaniline
https://huagongshe.com/reaction/1468098
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-2-nitroaniline | HCID 74218 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloro-4-iodo-2-nitroaniline | HCID 22317548 | — |
Reaction Steps
To a solution of 5-chloro-2-nitroaniline (500 mg, 2.90 mmol) in acetic acid (20 ml) was added NIS (650 mg, 2.89 mmol). The resulting solution was stirred overnight at room temperature and then diluted with water (40 ml). The solids were collected by filtration to afford 5-chloro-4-iodo-2-nitroaniline as a brown solid (800 mg, crude). To a solution of 5-chloro-4-iodo-2-nitroaniline (800 mg, crude) in water (4 ml) and ethanol (20 ml) was added Fe powder (600 mg, 10.74 mmol) and ammonium chloride (430 mg, 8.04 mmol). The resulting solution was stirred overnight at reflux and then cooled to room temperature. The solid was filtered out and the filtrate was concentrated under vacuum. The residue was dissolved in ethyl acetate (200 ml) and washed with brine (100 ml), dried over Na2SO4 and concentrated under vacuum to afford 4-chloro-5-iodobenzene-1,2-diamine as a brown solid (600 mg, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000187B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-aff20b7e50be41e6b4d92ab91748efcf |
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| Source note | uspto-grants-2015_04 |
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