HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579933Generated: October 30, 2026
Acetophenone → N,N-diethyl-4-(1-phenylethenyl)aniline
https://huagongshe.com/reaction/579933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Benzenamine, 4-bromo-N,N-diethyl- | HCID 16328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178463831 | HCID 178463831 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-diethyl-4-(1-phenylethenyl)aniline | HCID 14150475 | — |
Reaction Steps
After adding dropwise 100 ml of a benzene solution containing 8 g of acetophenone to a tetrahydrofuran solution of 4-diethylaminophenylmagnesium bromide prepared from 2 g of magnesium, 16 g of 4-bromodiethylaniline, and 100 ml of tetrahydrofuran, stirring was continued under reflux for 5 hours. After cooling, 200 ml of a saturated aqueous ammonium chloride solution was added thereto. The mixture was subjected to hydrolysis, and an organic layer was separated and washed with water. After distilling off the solvent, the residue was dissolved in benzene, and the solution was stirred and refluxed with the addition of 0.1 g of p-toluenesulfonic acid for one hour. After distilling off the solvent, the residue was dissolved in benzene, and the product was separated and purified by silica gel column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04751163 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-960e4de827e14df2b3b7e25a1300cacf |
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| Source note | uspto-grants-1988_06 |
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