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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398277Generated: November 1, 2026

N,N-Dimethylaniline → 3,5-Dichloro-2',4-dihydroxy-5'-fluorobenzanilide

https://huagongshe.com/reaction/2398277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Fluorosalicylic acidHCID 67658—
Reactant4-Amino-2,6-dichlorophenolHCID 80037—
SolventBenzeneHCID 241—
Product3,5-Dichloro-2',4-dihydroxy-5'-fluorobenzanilideHCID 2032754155%

Reaction Steps

5-Fluorosalicylic acid (5.15 g.) and 3,5-dichloro-4-hydroxyaniline (5.88 g.) were well mixed to which was added benzene (10 ml.) and N,N-dimethylaniline (4.35 ml.). Then with stirring thionyl chloride (3.3 ml.) was added and refluxed 30 minutes. The resulting solution was evaporated and the residue was dissolved in ethyl acetate and subjected to decolorization with activated charcoal followed by washing with 2 N hydrochloric acid and 2.5% sodium bicarbonate solution. The ethyl acetate was then extracted several times with 2 N sodium carbonate solution and the aqueous extracts were combined and brought to pH 1-2 with hydrochloric acid to give a precipitate which was recrystallized from aqueous acetone to give white needle-like crystals (5.7 g.) of 3,5-dichloro-2',4-dihydroxy-5'-fluorobenzanilide. Yield: 55%. Melting point: 227°-229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024253
Source datasetuspto-grants-1977_05
ORD IDord-66211cfa472d4bd9a1199fbc1b3a3a5b
Source noteuspto-grants-1977_05