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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419667Generated: November 1, 2026

Sodium hydride → 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene

https://huagongshe.com/reaction/1419667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTrimethylphosphonium bromideHCID 22062633—
Reactant4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehydeHCID 22617091—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-[N,N-bis(3,4-dimethylphenyl)amino]styreneHCID 1089278385%

Reaction Steps

Into a three-necked flask, 12.1 g of sodium hydride and 580 ml of 1,2-dimethoxyethane were placed, and 108.5 g of trimethylphosphonium bromide was added thereto with stirring at room temperature. Next, after a drop of absolute alcohol was added, the reaction was allowed to proceed at 70° C. for 4 hours. Then, 100.0 g of 4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehyde was added to the reaction mixture, to carry out reaction at 70° C. for 5 hours, followed by filtration to collect a cake. The cake was extracted with ether and the extract was put together with the filtrate and washed with water. Then, the ether solution was dehydrated with calcium chloride, and thereafter the ether was removed to obtain a crude product. After twice recrystallized from ethanol, acicular 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene was obtained in an amount of 84.5 g (yield: 85.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05888690
Source datasetuspto-grants-1999_03
ORD IDord-5332db7517f64ea9b68a75fc1487d923
Source noteuspto-grants-1999_03