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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110852Generated: November 2, 2026

Maleic Anhydride → HCID 14181821, compound

https://huagongshe.com/reaction/1110852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
Reactant4-FluoroanilineHCID 9731—
ReactantAcetyl bromideHCID 10482—
SolventTolueneHCID 1140—
ProductHCID 14181821HCID 14181821—

Reaction Conditions

Temperature30 °C

Reaction Steps

29.4 g. (0.3 mole) maleic acid anhydride were dissolved in 300 ml. toluene and a solution of 33.3 g. (0.3 mole) 4-fluoroaniline in 100 ml. toluene added thereto at 30° C. The hemi-anilide rapidly precipitated out. For the completion of the reaction, the mixture was heated for 2 hours to 100° C., then cooled, the precipitated product filtered off, washed and dried. The yield of hemi-anilide was quantitative. The hemianilide was suspended in acetic acid ethyl ester and 43 g. (0.35 mole) acetyl bromide added thereto. The reaction was carried out by stirring at 30° C. (2 hrs.) and by subsequent 2 hours heating to reflux, thereafter the solvent was distilled off and the residue crystallised. The yield amounted to 69.2 g. (corresponding to 85.5% of theory). The product displayed a melting point of 154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977183
Source datasetuspto-grants-1990_12
ORD IDord-59297a8ec08b474ea4c9265f0ce420a6
Source noteuspto-grants-1990_12