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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414332Erstellt: 24. Oktober 2026

Ethylamine → 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/414332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylamineHCID 6341—
EduktNitroethaneHCID 6587—
EduktImidazo[1,2-a]pyridine-6-carbaldehydeHCID 7164582—
KatalysatorButylamineHCID 8007—
LösungsmittelEthanolHCID 702—
Produkt6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridineHCID 5391556811,9%

Reaktionsschritte

In 40 ml of ethanol, 6.9 g of 6-imidazo[1,2-a]pyridinecarbaldehyde was stirred under reflux for 14 hours, together with 10.6 g of nitroethane and 30 drops of n-butyl amine. Then, a small quantity of ethyl amine was added thereto and the mixture was stirred under reflux for further 18 hours. After insoluble matter was removed by filtration upon heating, 50 ml of ethanol and 150 ml of ether were further added to remove insoluble matter by filtration. The solvent was removed by distillation under reduced pressure and the residue was recrystallized twice from ethanol to obtain 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04791203
Quelldatensatzuspto-grants-1988_12
ORD IDord-57882014ec2d410fa092ab3358781700
Quellennotizuspto-grants-1988_12