Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Chlorobenzylamine | HCID 66036 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Ethyl 2-cyano-2-(hydroxyimino)acetate | HCID 6399078 | — |
| Edukt | 1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1) | HCID 12221228 | — |
| Edukt | 2-[(4-Chlorophenyl)methyl]amino-2-imidazoline | HCID 13785676 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178508072 | HCID 178508072 | 77% |
Reaktionsschritte
To a solution of 62.30 g. 0.44 mol) of 4-chlorobenzylamine in 500 ml absolute EtOH (dried over 4A molecular sieve aluminosilicate desiccant) is added 107.40 g (0.44 mol) 2-(methylthio)-2-imidazoline hydroiodide. The mixture is heated to boiling on a steam bath in an open flask and about 150 ml of the ethanol is allowed to slowly boil off over 2 hr. This solution is added while still hot to 1.76 mole of sodium ethoxide in 1650 ml absolute EtOH. To the resulting stirred, basic solution of 2-[(4-chlorophenyl)methyl]amino-2-imidazoline is then added 61.85 g (0.44 mol) crystalline (mp 129°-131°) ethyl oximinocyanoacetate in portions. The bright yellow solution is refluxed for 3 hr and then cooled to room temperature. The yellow precipitate is collected, washed with i-PrOH, and partially air-dried. The damp sodium salt is dissolved in 2000 ml H2O and acidified with glacial HOAc. The bright pink precipitate is filtered and aid-dried overnight, then oven-dried in vacuo at 100° to yield 103.05 g (77%) of pink powder, mp 238°-241°d. Recrystallization of this material from DMF-EtOH gives red crystals, mp 241°d.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04642345 |
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| Quelldatensatz | uspto-grants-1987_02 |
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| ORD ID | ord-ce8f3c4488e14b6eb59bfdfb901c4901 |
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| Quellennotiz | uspto-grants-1987_02 |
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