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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2397603Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/2397603

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt4-Bromo-2,6-xylidineHCID 90549—
EduktSodium FormateHCID 2723810—
KatalysatorHexadecyltrimethylammonium BromideHCID 5974—
KatalysatorPalladiumHCID 23938—
LösungsmittelWaterHCID 962—
Produkt3,3',5,5'-TetramethylbenzidineHCID 4120663,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04022795
Quelldatensatzuspto-grants-1977_05
ORD IDord-e442844c76fd4e4d833b347290a3306d
Quellennotizuspto-grants-1977_05