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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397603Generated: October 26, 2026

Sodium Hydroxide → 3,3',5,5'-Tetramethylbenzidine

https://huagongshe.com/reaction/2397603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-2,6-xylidineHCID 90549—
ReactantSodium FormateHCID 2723810—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product3,3',5,5'-TetramethylbenzidineHCID 4120663.3%

Reaction Steps

4-Bromo-2,6-dimethylaniline (24.0 parts), 3% palladium on charcoal (50% paste; 2.0 parts), cetyltrimethylammonium bromide (4.0 parts), sodium hydroxide liquor (32%; 13.5 parts), sodium formate (6.8 parts) in water (60 parts) are stirred at the boil under reflux for 3 hours. Sodium formate (6.8 parts is then added and the mixture boiled for 3 hours when a further charge of sodium formate (6.8 parts) is made. The reaction mixture is then held at the boil under reflux for a further 23 hours. The mixture is then steam distilled and from the distillate 2.2 parts (18.2%) of 2,6-dimethylaniline is recovered by extraction with ether. The reaction mixture after steam distillation is cooled to room temperature and then filtered. The residue is extracted continuously with methanol (60 parts) for 5 hours and then the extract cooled. The colourless crystalline precipitate is filtered off and dried to give 7.7 parts (63.3%) of 3,3',5,5'-tetramethyl benzidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022795
Source datasetuspto-grants-1977_05
ORD IDord-e442844c76fd4e4d833b347290a3306d
Source noteuspto-grants-1977_05