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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantBenzenamine, 4-bromo-N,N-diethyl-HCID 16328—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178463831HCID 178463831—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diethyl-4-(1-phenylethenyl)anilineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751163
Source datasetuspto-grants-1988_06
ORD IDord-960e4de827e14df2b3b7e25a1300cacf
Source noteuspto-grants-1988_06