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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843303Generated: October 26, 2026

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

https://huagongshe.com/reaction/843303

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 numberUS06376695B1
Source datasetuspto-grants-2002_04
ORD IDord-81e3f6e1782d4a588d1632b017139fcd
Source noteuspto-grants-2002_04