HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400603Generated: October 25, 2026
Methyl 4-iodo-3-nitrobenzoate → Methyl 3-amino-4-iodobenzoate
https://huagongshe.com/reaction/400603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-iodo-3-nitrobenzoate | HCID 297884 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 3-amino-4-iodobenzoate | HCID 21628210 | 88.8% |
Reaction Steps
A solution of 4-iodo-3-nitrobenzoic acid methyl ester (2.0 g, 6.50 mmol) in 25 mL of absolute alcohol and 15 mL of glacial acetic acid was treated with iron powder (3.6 g, 65.0 mmol) and the mixture was heated at 80° C. After 1 hour, the reaction mixture was filtered through a pad of silica, washed with ethanol, and concentrated in vacuo. The residue was diluted with a solution of potassium carbonate and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give 1.6 g of 3-amino-4-iodobenzoic acid methyl ester as a white solid (88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741897B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-7d5b4f8cd506480dacb0dc38b550ddf1 |
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| Source note | uspto-grants-2014_06 |
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