Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47238Erstellt: 23. Oktober 2026

Formaldehyde → HCID 68835881, Verbindung

https://huagongshe.com/de/reaction/47238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Edukt1-MethylpiperazineHCID 53167—
Edukt(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
LösungsmittelEthanolHCID 702—
ProduktHCID 68835881HCID 6883588121%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120 mg, 0.57 mmol), paraformaldehyde (17 mg, 0.57 mmol), and 1-methylpiperazine (63 μL, 0.57 mmol) in 4.0 mL EtOH was heated at reflux for 6.5 h. After standing at room temperature for 23 h, the mixture was concentrated to 3 mL solvent and 1 mL of hexane added. The resulting solution was cooled to 0° C. and the yellow solid which formed was collected by filtration. The solid collected was partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate. The organic layer was removed and the aqueous layer washed with ethyl acetate (15 mL). The aqueous layer was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried with Na2SO4. The organic layer was concentrated and the residue was crystallized from ethyl acetate/hexane to give the title compound (38 mg, 21%) as a bright yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699863B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-071b76b7dc524e829eb7e50af8cf8210
Quellennotizuspto-grants-2004_03