Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetanilide | HCID 904 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | N-(4-Butyrylphenyl)acetamide | HCID 4304236 | — |
Reaction Steps
81.3 g of acetanilide are suspended in 600 ml of carbon disulphide and 76.7 g of butyryl chloride and, in portions, 198 g of aluminium trichloride are added while stirring. The mixture is stirred for some time at 30°-35° and heated at the boil for 18 hours. It is then allowed to cool, stirred into 200 ml of ice-water and extracted twice with 500 ml of ethyl acetate each time. The organic phases are combined, washed with 500 ml of additional acid and twice with 500 ml of 15% strength sodium carbonate solution each time, dried over magnesium sulphate and concentrated to 150 ml under reduced pressure. The residue obtained by concentration is allowed to cool, filtered with suction, washed twice with diethyl ether and dried under reduced pressure. p-Acetaminobutyrophenone having a melting point of 141°-143° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04476132 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-1ce821c7e8364b84b48f59e3ae4ba77e |
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| Source note | uspto-grants-1984_10 |
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