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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247112Erstellt: 24. Oktober 2026

N-Methylbenzylamine → 5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazole

https://huagongshe.com/de/reaction/247112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylbenzylamineHCID 7669—
EduktTriethylamineHCID 8471—
Edukt5-Acetonyl-3-chloromethyl-1,2,4-oxadiazoleHCID 13824705—
EduktChloroform methanolHCID 21584188—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazoleHCID 2016125665,6%

Reaktionsschritte

A mixture of 800 mg of 5-acetonyl-3-chloromethyl-1,2,4-oxadiazole, 720 mg of N-methylbenzylamine and 1.0 g of triethylamine in 5 ml of DMF was stirred at room temperature for 8 hours. The reaction mixture was then poured into ice-water and the resultant mixture was extracted with ethyl acetate. The extracts were washed with water, dried over magnesium sulfate and concentrated in vacuo to yield a brown oil. Chromatography on silica gel using chloroform-methanol (20:1, v/v) as eluent afforded 780 mg of 5-acetonyl-3-(N-benzyl-N-methylamino)methyl-1,2,4-oxadiazole as a colorless oil, IR νmaxneat cm-1 : 1730, 1635, 1580, 1545, 1450, 1360.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04705786
Quelldatensatzuspto-grants-1987_11
ORD IDord-303c850ae3a546e8b488f5e8da837353
Quellennotizuspto-grants-1987_11