HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399455Generated: October 31, 2026
2-(3-Fluoro-4-nitrobenzamido)acetic acid → 2-(4-Amino-3-fluorobenzamido)acetic acid
https://huagongshe.com/reaction/1399455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(3-Fluoro-4-nitrobenzamido)acetic acid | HCID 15925739 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Amino-3-fluorobenzamido)acetic acid | HCID 15925741 | 71% |
Reaction Steps
To a suspension of iron powder (231 mg, 4.13 mmol) in AcOH (2 mL) was added 2-(3-fluoro-4-nitrobenzamido)acetic acid (100 mg, 0.413 mmol) at rt and stirred at 85-90° C. for 15 min. The reaction mixture was attained to rt and diluted with EtOAc (20 mL). The solution was stirred for 5 min and filtered through celite. The celite bed was washed with EtOAc (10 mL) and the combined organic layer was evaporated under reduced pressure. The residue was chromatographed over silica gel column using chloroform:methanol (70:30) as eluents to give the product as an off-white color solid (62 mg, 71%), 198-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906344B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-b243069e5cc0469dbbf7a5c0767c2291 |
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| Source note | uspto-grants-2014_12 |
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