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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078012Generated: November 2, 2026

Acetic Acid → 4'-Amino-2'-fluoro-5'-(o-methoxyanilino)acetanilide

https://huagongshe.com/reaction/1078012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2'-Fluoro-5'-(o-methoxyanilino)-4'-nitroacetanilideHCID 15346064—
CatalystIronHCID 23925—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4'-Amino-2'-fluoro-5'-(o-methoxyanilino)acetanilideHCID 15346065—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545742
Source datasetuspto-grants-1996_08
ORD IDord-b516a13421474b5cb1c3b6bcf9845312
Source noteuspto-grants-1996_08