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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632509Generated: October 26, 2026

Acetanilide → N-(4-Butyrylphenyl)acetamide

https://huagongshe.com/reaction/1632509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetanilideHCID 904—
ReactantButyryl chlorideHCID 8855—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
ProductN-(4-Butyrylphenyl)acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04476132
Source datasetuspto-grants-1984_10
ORD IDord-1ce821c7e8364b84b48f59e3ae4ba77e
Source noteuspto-grants-1984_10