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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 4-(Pyridin-4-yl)aniline | HCID 1512654 | — |
| Reactant | Crotonic anhydride | HCID 6049834 | — |
| Reactant | N-[4-(4-pyridinyl)phenyl]-2-butenamide methanesulfonate | HCID 86738821 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[4-(4-pyridinyl)phenyl]-2-butenamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377585 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-52efe3b405e9423abe39205f6c0af158 |
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| Source note | uspto-grants-1983_03 |
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