Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235995Erstellt: 24. Oktober 2026

4-Chlorobenzylamine → HCID 178508072, Verbindung

https://huagongshe.com/de/reaction/235995

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorobenzylamineHCID 66036—
EduktSodium ethoxideHCID 2723922—
EduktEthyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
Edukt1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1)HCID 12221228—
Edukt2-[(4-Chlorophenyl)methyl]amino-2-imidazolineHCID 13785676—
LösungsmittelEthanolHCID 702—
ProduktHCID 178508072HCID 17850807277%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04642345
Quelldatensatzuspto-grants-1987_02
ORD IDord-ce8f3c4488e14b6eb59bfdfb901c4901
Quellennotizuspto-grants-1987_02