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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478976Generated: November 3, 2026

Hydrochloric Acid → 1,4-Bis(4-di(4-bromophenyl)aminostyryl)benzene

https://huagongshe.com/reaction/1478976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-(Bis(4-bromophenyl)amino)benzaldehydeHCID 18668904—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 178476836HCID 178476836—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product1,4-Bis(4-di(4-bromophenyl)aminostyryl)benzeneHCID 76597930—

Reaction Steps

A solution of 37.8 g (100 mmol) of p-xylene diethylphosphonate in 200 ml of DMF is added to a suspension, cooled to 0° C., of 38.5 g (400 mmol) of sodium tert-butoxide in 1000 ml of anhydrous DMF. After the mixture has been stirred for a further 30 min., a solution of 90.5 g (210 mmol) of bis(4-bromophenyl)(4-formylphenyl)amine in 300 ml of DMF is added over the course of 30 min., the mixture is stirred at 0° C. for a further 4 h, and then 500 ml of 1N hydrochloric acid and 300 ml of ethanol are added. The solid is filtered off with suction, washed three times with 300 ml of water and three times with 200 ml of ethanol and dried under reduced pressure. The product is subsequently recrystallised from DMF, filtered off with suction, washed three times with 200 ml of ethanol and dried under reduced pressure. Yield: 86.1 g (92 mmol), 92.3% of theory; purity: 99% according to 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403849B2
Source datasetuspto-grants-2016_08
ORD IDord-2f9c63735ce74f739666432a435728d5
Source noteuspto-grants-2016_08