HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584283Generated: October 31, 2026
Acetic Acid → Benzenamine, 3-bromo-4-methyl-
https://huagongshe.com/reaction/584283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Bromo-4-nitrotoluene | HCID 82189 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenamine, 3-bromo-4-methyl- | HCID 82187 | 100% |
Reaction Steps
30 g (139 mmol) of 2-bromo-4-nitrotoluene are placed in 180 ml of water, 400 ml of ethanol and 110 ml of acetic acid in a round-bottomed flask and under a stream of nitrogen. The medium is heated to 70° C. and 31 g (556 mmol) of iron are added portionwise. The mixture is refluxed for 2 hours and, after cooling, 180 ml of 34% aqueous ammonia are added slowly. The mixture is filtered through Celite and the organic phase is extracted with water and ethyl acetate. It is then dried over magnesium sulfate, filtered and then evaporated. 25.5 g (100%) of the expected product are obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924400B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-e312b2f9061442c5b2573add0e031ecb |
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| Source note | uspto-grants-2005_08 |
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