HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629294Generated: October 29, 2026
Acetic Acid → 4-Bromo-5-(2,4-difluorophenoxy)benzene-1,2-diamine
https://huagongshe.com/reaction/629294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Bromo-5-(2,4-difluorophenoxy)-2-nitroaniline | HCID 118093668 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-5-(2,4-difluorophenoxy)benzene-1,2-diamine | HCID 118093676 | 99.8% |
Reaction Steps
A suspension of 4-bromo-5-(2,4-difluorophenoxy)-2-nitroaniline (0.406 g, 1.18 mmol) in tetrahydrofuran (5.0 mL) was treated with iron (0.657 g, 11.8 mmol), followed by acetic acid (4.9 mL, 87 mmol) and stirred at 60° C. for 1 h. The reaction mixture was diluted with ethyl acetate and quenched carefully with saturated sodium bicarbonate. The organic layer was separated and washed again with saturated sodium bicarbonate and brine, dried with magnesium sulfate, filtered, and concentrated to give the desired product (371 mg, quantitative) that was used immediately without further purification. LCMS calculated for C12H10BrF2N2O (M+H)+: m/z=315.0, 317.0. found: 315.0, 316.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315501B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-26b489fef1bc4ac395a040371148d955 |
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| Source note | uspto-grants-2016_04 |
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