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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354842Generated: October 30, 2026

Chloroform → N-[4-(4-pyridinyl)phenyl]-2-butenamide

https://huagongshe.com/reaction/354842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant4-(Pyridin-4-yl)anilineHCID 1512654—
ReactantCrotonic anhydrideHCID 6049834—
ReactantN-[4-(4-pyridinyl)phenyl]-2-butenamide methanesulfonateHCID 86738821—
SolventDimethylformamideHCID 6228—
ProductN-[4-(4-pyridinyl)phenyl]-2-butenamideHCID 54510060—

Reaction Steps

A mixture containing 6.8 g. of 4-(4-pyridinyl)benzeneamine, 17.8 ml. of crotonic anhydride and 200 ml. of chloroform was stirred at room temperature for 2 hours and then under reflux for 16 hours. The suspension was filtered and the filtercake was suspended in water plus ammonium hydroxide solution and was refiltered to give 3.86 g. of light tan solid after air-drying on the funnel. The chloroform filtrate was concentrated in vacuo and the tan residue was suspended in a mixture of water and ammonium hydroxide and the mixture filtered to give more tan solid. The combined tan solids were taken up in dimethylformamide, the hot solution filtered and the filtrate concentrated to less than 300 ml. and then treated with a slight excess of methanesulfonic acid in ethanol. The resulting mixture was diluted with ether and the separated product was collected and dried in vacuo at 125° C. for 14 hours to yield 4.31 g. of N-[4-(4-pyridinyl)phenyl]-2-butenamide methanesulfonate, m.p. 247°-249° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377585
Source datasetuspto-grants-1983_03
ORD IDord-52efe3b405e9423abe39205f6c0af158
Source noteuspto-grants-1983_03