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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromo-2,6-xylidine | HCID 90549 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,3',5,5'-Tetramethylbenzidine | HCID 41206 | 63.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04022795 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-e442844c76fd4e4d833b347290a3306d |
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| Source note | uspto-grants-1977_05 |
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