HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182263Generated: November 1, 2026
1-Bromo-2,4-dimethyl-3-nitrobenzene → 3-Bromo-2,6-dimethylaniline
https://huagongshe.com/reaction/1182263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2,4-dimethyl-3-nitrobenzene | HCID 2753380 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Bromo-2,6-dimethylaniline | HCID 12792330 | — |
Reaction Steps
To a solution of crude 1-bromo-2,4-dimethyl-3-nitrobenzene (0.58 g, 2.9 mmol) in glacial acetic acid (12 mL) was added iron powder (0.65 g, 11.6 mmol). The mixture was stirred rapidly at 80° C. under nitrogen for 2 hours. Upon completion, the mixture was cooled, diluted with diethyl ether and extracted with aqueous sodium hydroxide solution (2N). The organic layer was dried over sodium sulfate, decanted and concentrated under reduced pressure to give 3-bromo-2,6-dimethylphenylamine as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288538B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-21c746c8382246fc89d74d11dd98c0e2 |
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| Source note | uspto-grants-2007_10 |
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