HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871644Generated: November 1, 2026
Ethyl Acetate → 1-(4-pyridin-2-yl-phenyl)-ethanone
https://huagongshe.com/reaction/1871644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(2-Pyridyl)benzonitrile | HCID 1515238 | — |
| Reactant | HCID 178467822 | HCID 178467822 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-pyridin-2-yl-phenyl)-ethanone | HCID 10965472 | — |
Reaction Steps
After 21 ml of a 3M methyl magnesium bromide-diethyl ether solution was added dropwise to a solution of 3.10 g of 4-(2-pyridyl)benzonitrile in 120 ml of dichloromethane under ice-cooling in a nitrogen atmosphere, the mixture was stirred at room temperature for 20 hours. After the reaction, an aqueous ammonium chloride solution and ethyl acetate were added to the reaction mixture, followed by stirring of the resulting mixture. The ethyl acetate layer was separated from the reaction mixture, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate:hexane=1:2) to obtain the crude desired compound as crystals. Further, the crude compound was washed with diisopropyl ether-hexane to obtain 1.56 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06103907 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-6e4520d77c11416c805248261a060693 |
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| Source note | uspto-grants-2000_08 |
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