HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Bromide ion → N,N,N',N'-Tetramethylbenzidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Bromide ion | HCID 259 | — |
| Edukt | HCID 178482849 | HCID 178482849 | — |
| Produkt | N,N,N',N'-Tetramethylbenzidine | HCID 9702 | 70% |
Reaktionsschritte
A mixture of p-dimethylaminophenyl magnesium bromide (1 mole) and thallous bromide (2 moles) is stirred and refluxed under nitrogen for 5 hours. The cooled solution is filtered to remove thallium, and hydrogen chloride passed into the filtrate. The colorless hydrochloride which precipitates is filtered off, stirred into dilute sodium hydroxide, and the tetramethylbenzidine extracted with ether-benzene (1:1, 2 × 30 ml.) The extracts are dried over anhydrous sodium sulfate and the solvent removed to leave a yellow solid which is sublimed at 165°/0.05 mm. to give a 70% yield of pure N,N,N',N'-tetramethylbenzidine as a colorless solid, m.p. 195°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04020073 |
| Quelldatensatz | uspto-grants-1977_04 |
| ORD ID | ord-b0d7dbf2c85a46ec8aa432c160c0447e |
| Quellennotiz | uspto-grants-1977_04 |