HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259743Generated: October 30, 2026
Acetic Acid → 4'-Amino-2'-fluoro-5'-(o-methoxyanilino)acetanilide
https://huagongshe.com/reaction/259743
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 15346064 | HCID 15346064 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-Amino-2'-fluoro-5'-(o-methoxyanilino)acetanilide | HCID 15346065 | — |
Reaction Steps
A mixture of 2'-fluoro-5'-(o-methoxyanilino)-4'-nitroacetanilide (14.6 g, 0.046 mol) in ethyl acetate is slowly added to a mixture of iron powder (7.65 g, 0.137 mol) in a 5% acetic acid solution at 65° C. After the addition is complete, the reaction mixture is heated at 65° C. overnight, treated with additional iron powder (2.55 g), heated at 65° C. for one hour and filtered. The resultant filtrate is extracted with ethyl acetate. The organic extracts are combined, washed sequentially with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a brown oil. Flash column chromatography of the oil using silica gel and 10% to 30% ethyl acetate in methylene chloride solutions gives the title product as a brown oil which is identified by NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05523277 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-723147adf55f4e7fa529719b4ff7653e |
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| Source note | uspto-grants-1996_06 |
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