HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46634Erstellt: 24. Oktober 2026
N-Methylethylenediamine → N-(Diphenylmethyl)-1-methyl-4,5-dihydro-1H-imidazol-2-amine
https://huagongshe.com/de/reaction/46634
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Methylethylenediamine | HCID 8014 | — |
| Edukt | HCID 178504030 | HCID 178504030 | — |
| Lösungsmittel | 1,2-Dichlorobenzene | HCID 7239 | — |
| Produkt | N-(Diphenylmethyl)-1-methyl-4,5-dihydro-1H-imidazol-2-amine | HCID 12503394 | — |
Reaktionsschritte
To 7.41 grams (0.10 mole) of N-methylethylenediamine was added 38.43 grams (0.10 mole) of 1-(diphenylmethyl)-2-methyl-2-thiopseudourea hydroiodide in 250 milliliters of o-dichlorobenzene and the resulting mixture allowed to reflux overnight to produce the desired 2-diphenylmethylamino-1-methyl-2-imidazoline product. After completion of the heating, the solvent was removed by decantation and the residue purified by first dissolving in methanol containing activated carbon, replacing the methanol with isopropanol and diluting the isopropanol with acetone-ether to precipitate 16.55 grams (65 percent yield) of 2-diphenylmethylamino-1-methyl-2-imidazoline hydroiodide, m.p. 226°-228° C. After purification by treating with activated charcoal in methanol and recrystallizations from methanol-isopropanol, the product melted at (225°) 227°-229° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04174401 |
|---|
| Quelldatensatz | uspto-grants-1979_11 |
|---|
| ORD ID | ord-8e0652bcc7e64582be1d18a1658581e3 |
|---|
| Quellennotiz | uspto-grants-1979_11 |
|---|