Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14181821 | HCID 14181821 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04977183 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-59297a8ec08b474ea4c9265f0ce420a6 |
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| Source note | uspto-grants-1990_12 |
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